EP3412305B1 - Traitement d'une maladie de la coagulation par l'administration du fvw recombinant - Google Patents

Traitement d'une maladie de la coagulation par l'administration du fvw recombinant Download PDF

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EP3412305B1
EP3412305B1 EP18173179.5A EP18173179A EP3412305B1 EP 3412305 B1 EP3412305 B1 EP 3412305B1 EP 18173179 A EP18173179 A EP 18173179A EP 3412305 B1 EP3412305 B1 EP 3412305B1
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var
rvwf
fviii
composition
administered
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EP3412305A1 (fr
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Friedrich Scheiflinger
Peter Dr. Turecek
Bruce EWENSTEIN
Wing Yen Wong
Tobias M. Suiter
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Takeda Pharmaceutical Co Ltd
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Baxalta GmbH
Baxalta Inc
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Priority to EP20216368.9A priority Critical patent/EP3858375B1/fr
Priority to DK20216368.9T priority patent/DK3858375T3/da
Priority to PL18173179T priority patent/PL3412305T3/pl
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/36—Blood coagulation or fibrinolysis factors
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/36—Blood coagulation or fibrinolysis factors
    • A61K38/37—Factors VIII
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
    • A61K47/10—Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/04—Antihaemorrhagics; Procoagulants; Haemostatic agents; Antifibrinolytic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00Ā -Ā A61K41/00

Definitions

  • Coagulation diseases such as von Willebrand Disease (VWD) and Hemophilia
  • VWD von Willebrand Disease
  • Hemophilia generally result from a deficiency in the coagulation cascade.
  • von Willebrand Disease refers to the group of diseases caused by a deficiency of von Willebrand factor. Von Willebrand factor helps blood platelets clump together and stick to the blood vessel wall, which is necessary for normal blood clotting.
  • Hemophilia A refers to a deficiency of Factor VIII activity
  • Hemophilia B refers to a Factor IX deficiency.
  • Current treatment for these coagulopathies includes a replacement therapy using pharmaceutical preparations comprising the normal coagulation factor.
  • VWF von Willebrand Factor
  • VWF is a glycoprotein circulating in plasma as a series of multimers ranging in size from about 500 to 20,000 kD.
  • the full length of cDNA of VWF has been cloned; the propolypeptide corresponds to amino acid residues 23 to 764 of the full length prepro-VWF (Eikenboom et al (1995) Haemophilia 1, 77 90).
  • Multimeric forms of VWF are composed of 250 kD polypeptide subunits linked together by disulfide bonds. VWF mediates the initial platelet adhesion to the sub-endothelium of the damaged vessel wall, with the larger multimers exhibiting enhanced hemostatic activity.
  • Multimerized VWF binds to the platelet surface glycoprotein Gp1b ā‡ , through an interaction in the Al domain of VWF, facilitating platelet adhesion. Other sites on VWF mediate binding to the blood vessel wall. Thus, VWF forms a bridge between the platelet and the vessel wall that is essential to platelet adhesion and primary hemostasis under conditions of high shear stress.
  • endothelial cells secrete large polymeric forms of VWF and those forms of VWF that have a lower molecular weight arise from proteolytic cleavage.
  • the multimers of exceptionally large molecular masses are stored in the Weibel-Pallade bodies of the endothelial cells and liberated upon stimulation by agonists such as thrombin and histamine.
  • the present invention provides methods and combinations for treating coagulation disease by administering recombinant von Willebrand Factor (rVWF) alone or in combination with recombinant Factor VIII (rFVIII) to a subject in need thereof, with the result that the in-vivo half-life of Factor VIII is increased.
  • rVWF von Willebrand Factor
  • rFVIII recombinant Factor VIII
  • the present invention provides recombinant Von Willebrand Factor for use in a method for treating Von Willebrand Disease Type 3, wherein the rVWF is a high molecular weight VWF multimer composition comprising at least 40% VWF decamers or higher order multimers.
  • methods of the invention include co-administering to the subject recombinant Von Willebrand Factor (rVWF) and recombinant Factor VIII (rFVIII).
  • rVWF Von Willebrand Factor
  • rFVIII recombinant Factor VIII
  • the rVWF and rFVIII are administered together in a single composition.
  • the subject is administered between 1.0 IU/kg VWF:RCo and 150 IU/kg VWF:RCo per dose.
  • the subject is administered between 2 IU/kg VWF:RCo and 50 IU/kg VWF:RCo per dose.
  • the subject is administered between 5 IU/kg VWF:RCo and 40 IU/kg VWF:RCo per dose.
  • the subject is administered between 10 IU/kg VWF:RCo and 20 IU/kg VWF:RCo per dose.
  • the rVWF used in methods of the invention is matured in vitro by treatment with Furin.
  • the rVWF is produced through expression in a Chinese Hamster Ovary (CHO cell culture).
  • the rFVIII and rVWF are produced through expression in the same cell culture.
  • the subject is administered rVWF no more than once every other day.
  • the subject is administered rVWF no more than twice a week.
  • the Factor VIII half-life is extended by about 5 hours.
  • the Factor VIII half-life is extended for at least 12 hours.
  • the Factor VIII half-life is extended for at least 24 hours.
  • the Factor VIII half-life is extended for at least 36 hours.
  • the Factor VIII half-life is extended for at least 48 hours.
  • the ratio of FVIII procoagulant activity (IU FVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) administered to the subject is between 2:1 and 1:4.
  • the ratio of FVIII procoagulant activity (IU FVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) administered to the subject is between 3:2 and 1:3.
  • the ratio of FVIII procoagulant activity (IU FVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) administered to the subject is between 1:1 and 1:2.
  • the ratio of FVIII procoagulant activity (IU FVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) administered to the subject is about 3:4.
  • the rVWF has a specific activity of about 20-150 mU/ ā‡ g.
  • the high molecular weight VWF multimer composition comprises at least 40% VWF decamers or higher order multimers.
  • the high molecular weight VWF multimer composition comprises at least 50% VWF decamers or higher order multimers.
  • the high molecular weight VWF multimer composition comprises at least 60% VWF decamers or higher order multimers.
  • the high molecular weight VWF multimer composition comprises at least 70% VWF decamers or higher order multimers.
  • the present invention provides a method for treating Von Willebrand Disease in a subject in need thereof, the method comprising: administering to the subject recombinant Von Willebrand Factor (rVWF) such that Factor VIII half-life is extended as compared to a subject administered plasma derived Von Willebrand Factor, wherein: (a) the rVWF has a higher specific activity than plasma derived Von Willebrand Factor, wherein the specific activity of rVWF is about 20-150 mU/ ā‡ g; and (b) the FVIII half-life is at least 1.5 times higher as compared to FVIII half-life in a subject administered plasma derived Von Willebrand Factor.
  • rVWF Von Willebrand Factor
  • the present invention provides a method for treating Von Willebrand Disease in a subject in need thereof, the method comprising: administering to the subject recombinant Von Willebrand Factor (rVWF) such that Factor VIII half-life is extended as compared to a subject administered plasma derived Von Willebrand Factor, wherein: (a) the rVWF is a high molecular weight VWF multimer composition comprising at least 20% VWF decamers or higher order multimers, (b) the rVWF has a higher specific activity than plasma derived Von Willebrand Factor, wherein the specific activity of rVWF is at least about 20-150 mU/ ā‡ g; and (c) the FVIII half-life is at least 1.5 times higher as compared to FVIII half-life in a subject administered plasma derived Von Willebrand Factor.
  • rVWF Von Willebrand Factor
  • the level of Factor VIII procoagulant activity (FVIII:C) in the plasma of the subject 24 hours post-administration of the rVWF is at least 90% of the level of FVIII:C activity present in the plasma 1 hour post-administration.
  • the level of Factor VIII procoagulant activity (FVIII:C) in the plasma of the subject 24 hours post-administration is at least 100% of the level of FVIII:C activity present in the plasma 1 hour post-administration.
  • the level of Factor VIII procoagulant activity (FVIII:C) in the plasma of the subject 36 hours post-administration is at least 80% of the level of FVIII:C activity present in the plasma 1 hour post-administration.
  • the level of Factor VIII procoagulant activity (FVIII:C) in the plasma of the subject 48 hours post-administration is at least 50% of the level of FVIII:C activity present in the plasma 1 hour post-administration.
  • the higher order rVWF multimers arc stable for at least 6 hours post-administration.
  • the higher order rVWF multimers are stable for at least 12 hours post-administration.
  • the higher order rVWF multimers are stable for at least 18 hours post-administration.
  • the higher order rVWF multimers are stable for at least 24 hours post-administration.
  • the higher order rVWF multimers are stable for at least 36 hours post-administration.
  • the higher order rVWF multimers are stable for at least 48 hours post-administration.
  • the higher order rVWF multimers are stable for at least 72 hours post-administration.
  • the present invention provides a method for treating Von Willebrand Disease in a subject in need thereof, the method comprising: administering to the subject recombinant Von Willebrand Factor (rVWF).
  • rVWF Von Willebrand Factor
  • the method comprises co-administering to the subject recombinant Factor VIII (rFVIII) and recombinant Von Willebrand Factor (rVWF).
  • rFVIII recombinant Factor VIII
  • rVWF Von Willebrand Factor
  • the rFVIII and rVWF are administered together in a single composition.
  • the ratio of rFVIII procoagulant activity (IU rFVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) administered to the subject is between 2:1 and 1:4.
  • the ratio of rFVIII procoagulant activity (IU rFVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) administered to the subject is between 3:2 and 1:3.
  • the ratio of rFVIII procoagulant activity (IU rFVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) administered to the subject is between 1:1 and 1:2.
  • the ratio of rFVIII procoagulant activity (IU rFVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) administered to the subject is about 3:4.
  • the rVWF is matured in vitro by treatment with Furin.
  • the rVWF is expressed in mammalian cell culture.
  • the rFVIII is expressed in mammalian cell culture.
  • the mammalian culture comprises CHO cells.
  • the rFVIII and rVWF are co-expressed in the same culture.
  • the rFVIII and rVWF are co-purified.
  • the rFVIII and rVWF are purified separately.
  • a rFVIII/rVWF complex is reconstituted prior to administration.
  • rVWF is treated with Furin prior to reconstituting the rFVIII/rVWF complex.
  • the reconstituted rFVIII/rVWF complex is treated with Furin.
  • the Furin is recombinant Furin.
  • the subject is administered rVWF no more than once daily.
  • the subject is administered rVWF no more than once every other day.
  • the subject is co-administered rVWF no more than once every third day.
  • the subject is administered rVWF no more than once every fourth day.
  • the subject is administered between 1.5 IU/kg FVIII:C and 150 IU/kg FVIII:C per dose.
  • the subject is administered between 10 IU/kg FVIII:C and 100 IU/kg FVIII:C per dose.
  • the subject is administered between 25 IU/kg FVIII:C and 75 IU/kg FVIII:C per dose.
  • the subject is administered between 40 IU/kg FVIII:C and 60 IU/kg FVIII:C per dose.
  • the level of Factor VIII procoagulant activity (FVIII:C) in the plasma of the subject 24 hours post-administration is at least 90% of the level of FVIII:C activity present in the plasma 1 hour post-administration.
  • the level of Factor VIII procoagulant activity (FVIII:C) in the plasma of the subject 24 hours post-administration is at least 100% of the level of FVIII:C activity present in the plasma 1 hour post-administration.
  • the level of Factor VIII procoagulant activity (FVIII:C) in the plasma of the subject 36 hours post-administration is at least 80% of the level of FVIII:C activity present in the plasma 1 hour post-administration.
  • the level of Factor VIII procoagulant activity (FVIII:C) in the plasma of the subject 48 hours post-administration is at least 50% of the level of FVIII:C activity present in the plasma 1 hour post-administration.
  • the rVWF administered to the subject has a HMW VWF multimer composition comprising at least 40% VWF decamers or higher order multimers.
  • the rVWF administered to the subject has a HMW VWF multimer composition comprising at least 50% VWF decamers or higher order multimers.
  • higher order rVWF multimers are stable in vitro for at least 3 hours post-administration.
  • higher order rVWF multimers are stable in vitro for at least 6 hours post-administration.
  • higher order rV WF multimers are stable in vitro for at least 24 hours post-administration.
  • higher order rVWF multimers are stable in vitro for at least 36 hours post-administration.
  • higher order rVWF multimers are stable in vitro for at least 72 hours post-administration.
  • endogenous FVIII activity is stabilized for at least 12 hours.
  • endogenous FVIII activity is stabilized for at least 24 hours.
  • endogenous FVIII activity is stabilized for at least 36 hours.
  • endogenous FVIII activity is stabilized for at least 48 hours.
  • endogenous FVIII activity is stabilized for at least 72 hours.
  • co-administered rFVIII activity is stabilized for at least 24 hours.
  • co-administered rFVIII activity is stabilized for at least 36 hours.
  • co-administered rFVIII activity is stabilized for at least 48 hours.
  • co-administered rFVIII activity is stabilized for at least 72 hours.
  • co-administered rFVIII activity is stabilized by extending the half-life of the rFVIII in vivo.
  • FVIII half-life is extended by about five hours as compared to a patient administered pdFVIII.
  • At least 1% of the co-administered rFVIII activity is maintained for at least 36 hours in a patient administered said rFVIII.
  • At least 1% of the co-administered rFVIII activity is maintained for at least 48 hours in a patient administered said rFVIII.
  • At least 1 % of the co-administered rFVIII activity is maintained for at least 72 hours in a patient administered said rFVIII.
  • At least 1% of the co-administered rFVIII activity is maintained for at least 90 hours in a patient administered said rFVIII.
  • At least 1% of the co-administered rFVIII activity is maintained for at least 120 hours in a patient administered said rFVIII.
  • At least 1% of the co-administered rFVIII activity is maintained for at least 168 hours in a patient administered said rFVIII.
  • the present invention provides compositions and methods for treating coagulation disease in a subject by administering recombinant von Willebrand Factor (rVWF) alone or in combination with Factor VIII (which can be recombinant or plasma derived).
  • rVWF von Willebrand Factor
  • Factor VIII which can be recombinant or plasma derived.
  • the compositions and methods of the present invention are used for treating von Willebrand Disease (VWD) type 3.
  • rVWF administered to the subject provides increased stability for in vivo Factor VIII (FVIII) activity as compared to FVIII stability due to administered plasma derived VWF, allowing for lower doses and/or frequency of treatment than in traditional treatments for coagulation diseases.
  • Increased stability of FVIII activity and levels of FVIII can be measured using methods known in the art and described herein, including standard assays such as one-stage clotting assays, chromogenic assays, and immunoassays (see for example Lippi et al., Blood Coagulation & Fibrinolysis, 2009, 20(1):1-3 and Chandler et al., Am J. Clin. Pathol., 2003, 120:34-39 ). As shown in FIG.
  • FIGs. 2 and 7 also show increases in FVIII activity in patients administered rVWF as compared to those administered pdVWF: FIG. 2 shows that average FVIII half-life was increased by 4.7 hours for patients administered rVWF as compared to patients administered pdVWF, and the data from Cohort 4A in FIG. 7 shows an increase in FVIII half-life of 5.3 hours for patients administered rVWF as compared to patients administered pdVWF.
  • the half-life of plasma FVIII is increased by 12.27 hours in VWD patients receiving rVWF in combination with rFVIII as compared to patients receiving FVIII (i.e., Advate) alone.
  • the administration of rVWF stabilizes endogenous and/or co-administered FVIII activity, with the result that the in vivo half-life and/or activity of FVIII is increased.
  • the rVWF and FVIII can be administered to the subject together in a single composition.
  • neither rVWF nor FVIII are modified with a water soluble polymer.
  • either the rVWF or FVIII or both are modified with a water soluble polymer.
  • the FVIII may be recombinant or plasma derived.
  • the rVWF administered to the subject is a high molecular weight multimer composition comprising decamers or higher order multimers of rVWF.
  • the use of rVWF compositions of the invention provide therapeutic flexibility to dose (or re-dose) with or without FVIII (recombinant or plasma derived).
  • the rVWF administered to the subject is a high molecular weight VWF multimer composition comprising at least 40% VWF decamers or higher order multimers.
  • the rVWF administered to subjects is not modified with a water soluble polymer.
  • the rVWF administered to the subject has a higher specific activity than pdVWF.
  • the rVWF alone or in combination with pdFVIII or rFVIII is administered to the subject no more than twice a week.
  • the rVWF is processed with Furin prior to administration to the subject. In certain embodiments, the rVWF is processed with recombinant Furin.
  • the rVWF of use in the present invention is produced in accordance with methods known in the art and described for example in US 2012/0035110, filed July 8, 2011 and US Patent No. 8,173,597, issued May 8, 2012 .
  • rVWF alone or in combination with FVIII is used to treat patients with VWD Patients with VWD have some level of FVIII, but the stability of that FVIII is generally compromised because these patients lack VWF.
  • Treatment of VWD patients may in some embodiments involve an initial treatment with both rVWF and rFVIII followed by repeated administrations of rVWF alone.
  • the initial treatment may be with rVWF alone while subsequent repeated administrations are with both rVWF and rFVIII, or the initial and subsequent repeat administrations may all include a co-administration of both rVWF and rFVIII.
  • the initial treatment may be rFVIII alone while the subsequent repeat treatments involve co-administration of rVWF and rFVIII.
  • rVWF refers to recombinant VWF.
  • rFVIII refers to recombinant FVIII.
  • recombinant when used with reference, e.g., to a cell, or nucleic acid, protein, or vector, indicates that the cell, nucleic acid, protein or vector, has been modified by the introduction of a heterologous nucleic acid or protein or the alteration of a native nucleic acid or protein, or that the cell is derived from a cell so modified.
  • recombinant cells express genes that are not found within the native (non-recombinant) form of the cell or express native genes that are otherwise abnormally expressed, under expressed or not expressed at all.
  • VWF proteins of the invention can comprise a construct, for example, prepared as in WO 1986/06096 published on Oct. 23, 1986 and U.S. patent application Ser. No. 07/559,509, filed on Jul. 23, 1990 , in the name of Ginsburg et al.
  • the VWF in the present invention can include all potential forms, including the monomeric and multimeric forms. It should also be understood that the present invention encompasses different forms of VWF to be used in combination.
  • the VWF of the present invention may include different multimers, different derivatives and both biologically active derivatives and derivatives not biologically active.
  • the recombinant VWF embraces any member of the VWF family from, for example, a mammal such as a primate, human, monkey, rabbit, pig, rodent, mouse, rat, hamster, gerbil, canine, feline, and biologically active derivatives thereof.
  • Mutant and variant VWF proteins having activity are also embraced, as are functional fragments and fusion proteins of the VWF proteins.
  • the VWF of the invention may further comprise tags that facilitate purification, detection, or both.
  • the VWF described herein may further be modified with a therapeutic moiety or a moiety suitable imaging in vitro or in vivo.
  • Plasmid-derived VWF includes all forms of the protein found in blood including the mature VWF obtained from a mammal having the property of in vivo-stabilizing, e.g. binding, of at least one FVIII molecule.
  • highly multimeric VWF or ā€œhigh molecular weight VWFā€ refers to VWF comprising at least 10 subunits, or 12, 14, or 16 subunits, to about 20, 22, 24 or 26 subunits or more.
  • subunit refers to a monomer of VWF. As is known in the art, it is generally dimers of VWF that polymerize to form the larger order multimers. ( see Turecek et al., Semin. Thromb. Hemost. 2010, 36(5): 510-521 ).
  • factor VIII refers to any form of factor VIII molecule with the typical characteristics of blood coagulation factor VIII, whether endogenous to a patient, derived from blood plasma, or produced through the use of recombinant DNA techniques, and including all modified forms of factor VIII.
  • Factor VIII (FVIII) exists naturally and in therapeutic preparations as a heterogeneous distribution of polypeptides arising from a single gene product ( see, e.g., Andersson ct al., Proc. Natl. Acad. Sci. USA, 83:2979-2983 (1986 )).
  • therapeutic preparations containing Factor VIII include those sold under the trade names of HEMOFIL M, ADVATE, and RECOMBINATE (available from Baxter Healthcare Corporation, Deerfield, Ill., U.S.A.).
  • Plasmid FVIII activity and "in vivo FVIII activityā€ are used interchangeably.
  • the in vivo FVIII activity measured using standard assays may be endogenous FVIII activity, the activity of a therapeutically administered FVIII (recombinant or plasma derived), or both endogenous and administered FVIII activity.
  • plasma FVIII refers to endogenous FVIII or administered recombinant or plasma derived FVIII.
  • von Willebrand Disease refers to the group of diseases caused by a deficiency of von Willebrand factor. Von Willebrand factor helps blood platelets clump together and stick to the blood vessel wall, which is necessary for normal blood clotting. As described in further detail herein, there are several types of Von Willebrand disease.
  • hemophilia refers to a group of disease states broadly characterized by reduced blood clotting or coagulation. Hemophilia may refer to Type A, Type B, or Type C hemophilia, or to the composite of all three diseases types.
  • Type A hemophilia (hemophilia A) is caused by a reduction or loss of factor VIII (FVIII) activity and is the most prominent of the hemophilia subtypes.
  • Type B hemophilia results from the loss or reduction of factor IX (FIX) clotting function.
  • Type C hemophilia is a consequence of the loss or reduction in factor XI (FXI) clotting activity.
  • Hemophilia A and B are X-linked diseases, while hemophilia C is autosomal.
  • Common treatments for hemophilia include both prophylactic and on-demand administration of clotting factors, such as FVIII, FIX, including BebulinĀ®-VH, and FXI, as well as FEIBA-VH, desmopressin, and plasma infusions.
  • isolated refers to material that is substantially or essentially free from components that normally accompany it as found in its native state. Purity and homogeneity are typically determined using analytical chemistry techniques such as polyacrylamide gel electrophoresis or high performance liquid chromatography. VWF is the predominant species present in a preparation is substantially purified.
  • purified in some embodiments denotes that a nucleic acid or protein gives rise to essentially one band in an electrophoretic gel. In other embodiments, it means that the nucleic acid or protein is at least 50% pure, more preferably at least 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98%, 99% or more pure.
  • Purify or ā€œpurificationā€ in other embodiments means removing at least one contaminant from the composition to be purified. In this sense, purification does not require that the purified compound be homogenous, e.g., 1 00% pure.
  • administering includes intravenous administration, intramuscular administration, subcutaneous administration, oral administration, administration as a suppository, topical contact, intraperitoneal, intralesional, or intranasal administration, or the implantation of a slow-release device, e.g., a mini-osmotic pump, to a subject.
  • Administration is by any route including parenteral, and transmucosal (e.g., oral, nasal, vaginal, rectal, or transdermal).
  • Parenteral administration includes, e.g., intravenous, intramuscular, intra-arteriole, intradermal, subcutaneous, intraperitoneal, intraventricular, and intracranial.
  • Other modes of delivery include, but are not limited to, the use of liposomal formulations, intravenous infusion, transdermal patches, etc.
  • a therapeutically effective amount or dose or ā€œtherapeutically sufficient amount or doseā€ or ā€œeffective or sufficient amount or doseā€ refer to a dose that produces therapeutic effects for which it is administered.
  • a therapeutically effective amount of a drug useful for treating hemophilia can be the amount that is capable of preventing or relieving one or more symptoms associated with hemophilia.
  • the exact dose will depend on the purpose of the treatment, and will be ascertainable by one skilled in the art using known techniques ( see, e.g., Lieberman, Pharmaceutical Dosage Forms (vols.
  • the terms "patientā€ and ā€œsubjectā€ are used interchangeably and refer to a mammal (preferably human) that has a disease or has the potential of contracting a disease.
  • the term "aboutā€ denotes an approximate range of plus or minus 10% from a specified value. For instance, the language ā€œabout 20%ā€ encompasses a range of 18-22%.
  • half-life refers to the period of time it takes for the amount of a substance undergoing decay (or clearance from a sample or from a patient) to decrease by half.
  • compositions of the invention are provided.
  • the present invention utilizes compositions comprising recombinant von Willebrand Factor (rVWF) for treatment of VWD.
  • the present invention utilizes rVWF in combination with Factor VIII (FVIII).
  • the co-administered FVIII may be recombinant (rFVIII) or plasma derived (pdFVIII).
  • the compositions of the present invention stabilize in vivo Factor VIII activity (also referred to herein as plasma Factor VIII activity) such that the in vivo half-life of Factor VIII is extended as compared to that in subjects that have not been administered rVWF or that have been administered pdVWF.
  • Measuring the extent to which rVWF stabilizes FVIII activity can be carried out using methods known in the art.
  • the level of FVIII activity can be measured by, for instance, one-stage clotting assays, chromogenic assays, and immunoassays (see for example Lippi et al., Blood Coagulation & Fibrinolysis, 2009, 20(1):1-3 , European Pharmacopoeia (Ph. Eur., 3.sup.rd Ed. 1997:2.7.4), and Chandler et al., Am J. Clin. Pathol., 2003, 120:34-39 ).
  • VWF proteins of the invention may comprise a construct, for example, prepared as in WO 1986/06096 published on Oct. 23, 1986 and U.S. patent application Ser. No. 07/559,509, filed on Jul. 23, 1990 , in the name of Ginsburg et al..
  • the VWF useful for the present invention includes all potential forms, including the monomeric and multimeric forms.
  • One particularly useful form of VWF are homo-multimers of at least two VWFs.
  • the VWF proteins may be either a biologically active derivative, or when to be used solely as a stabilizer for FVIII the VWF may be of a form not biologically active.
  • the present invention encompasses different forms of VWF to be used in combination.
  • a composition useful for the present invention may include different multimers, different derivatives and both biologically active derivatives and derivatives not biologically active.
  • VWF serves as a bridge between platelets and specific components of the extracellular matrix, such as collagen.
  • the biological activity of VWF in this process can be measured by different in vitro assays ( Turecek et al., Semin. Thromb. Hemost. 28: 149-160, 2002 ).
  • the ristocetin cofactor assay is based on the agglutination of fresh or formalin-fixed platelets induced by the antibiotic ristocetin in the presence of VWF.
  • the degree of platelet agglutination depends on the VWF concentration and can be measured by the turbidimetric method, e.g. by use of an aggregometer ( Weiss et al., J. Clin. Invest.
  • the second method is the collagen binding assay, which is based on ELISA technology ( Brown et Bosak, Thromb. Res. 43: 303-311, 1986 ; Favaloro, Thromb. Haemost. 83: 127-135, 2000 ).
  • a microliter plate is coated with type I or III collagen.
  • the VWF is bound to the collagen surface and subsequently detected with an enzyme-labeled polyclonal antibody.
  • the last step is the substrate reaction, which can be photometrically monitored with an ELISA reader.
  • the specific Ristocetin Cofactor activity of the VWF (VWF:RCo) of the present invention is generally described in terms of mU/ ā‡ g of VWF, as measured using in vitro assays.
  • the rVWF of the invention has a specific activity of at least about 20, 22.5, 25, 27.5, 30, 32.5, 35, 37.5, 40, 42.5, 45, 47.5, 50, 52.5, 55, 57.5, 60, 62.5, 65, 67.5, 70, 72.5, 75, 77.5, 80, 82.5, 85, 87.5, 90, 92.5, 95, 97.5, 100, 105, 110, 115, 120, 125, 130, 135, 140, 145, 150 or more mU/ ā‡ g.
  • rVWF used in the methods described herein has a specific activity of from 20 mU/ ā‡ g to 150 mU/ ā‡ g. In another embodiment, the VWF has a specific activity of from 30 mU/ ā‡ g to 120 mU/ ā‡ g. In another embodiment, the rVWF has a specific activity from 40 mU/ ā‡ g to 90 mU/ ā‡ g. In yet another embodiment, the rVWF has a specific activity selected from variations 1 to 133 found in Table 1 . Table 1. Exemplary embodiments for the specific activity of rVWF found in the compositions and used in the methods provided herein. (mU/ ā‡ g) (mU/ ā‡ g) (mU/ ā‡ g) 20 Var.
  • Var. 76 80-120 Var. 109 42.5 Var. 10 20-150 Var. 44 40-60 Var. 77 80-110 Var. 110 45 Var. 11 20-140 Var. 45 40-50 Var. 78 80-100 Var. 111 47.5 Var. 12 20-130 Var. 46 50-150 Var. 79 80-90 Var. 112 50 Var. 13 20-120 Var. 47 50-140 Var. 80 90-150 Var. 113 52.5 Var. 14 20-110 Var. 48 50-130 Var. 81 90-140 Var. 114 55 Var. 15 20-100 Var. 49 50-120 Var. 82 90-130 Var. 115 57.5 Var. 16 20-90 Var. 50 50-110 Var. 83 90-120 Var. 116 60 Var. 17 20-80 Var. 51 50-100 Var.
  • Var. 84 90-110 Var. 117 62.5 Var. 18 20-70 Var. 52 50-90 Var. 85 90-100 Var. 118 65 Var. 19 20-60 Var. 53 50-80 Var. 86 100-150 Var. 119 67.5 Var. 20 20-50 Var. 54 50-70 Var. 87 100-140 Var. 120 70 Var. 21 20-40 Var. 55 50-60 Var. 88 100-130 Var. 121 72.5 Var. 22 30-150 Var. 56 60-150 Var. 89 100-120 Var. 122 75 Var. 23 30-140 Var. 57 60-140 Var. 90 100-110 Var. 123 77.5 Var. 24 30-130 Var. 58 60-130 Var. 91 110-150 Var. 124 80 Var. 25 30-120 Var. 59 60-120 Var.
  • Var. 92 110-140 Var. 125 82.5 Var. 26 30-110 Var. 60 60-110 Var. 93 110-130 Var. 126 85 Var. 27 30-100 Var. 61 60-100 Var. 94 110-120 Var. 127 87.5 Var. 28 30-90 Var. 62 60-90 Var. 95 120-150 Var. 128 90 Var. 29 30-80 Var. 63 60-80 Var. 96 120-140 Var. 129 92.5 Var. 30 30-70 Var. 64 60-70 Var. 97 120-130 Var. 130 95 Var. 31 30-60 Var. 65 70-150 Var. 98 130-150 Var. 131 97.5 Var. 32 30-50 Var. 66 70-140 Var. 99 130-140 Var. 132 100 Var. 33 30-40 Var. 67 70-130 Var. 100 140-150 Var. 133 105 Var. 34 Var. Variation
  • the rVWF of the present invention is highly multimeric comprising about 10 to about 40 subunits.
  • the multimeric rVWF produced using methods of the present invention comprise about 10-30, 12-28, 14-26, 16-24, 18-22, 20-21 subunits.
  • the rVWF is present in multimers varying in size from dimers to multimers of over 40 subunits (> 10 million Daltons). The largest multimers provide multiple binding sites that can interact with both platelet receptors and subcndothclial matrix sites of injury, and are the most hemostatically active form of VWF. As shown in the multimer analysis in FIG.
  • rVWF compositions of the present invention are generally not exposed to ADAMTS13 and retain their highly multimeric structure.
  • a rVWF composition used in the methods described herein has a distribution of rVWF oligomers characterized in that 95% of the oligomers have between 6 subunits and 20 subunits.
  • the a rVWF composition has a distribution of rVWF oligomers characterized in that 95% of the oligomers have a range of subunits selected from variations 458 to 641 found in Table 2. Table 2. Exemplary embodiments for the distribution of rVWF oligomers found in the compositions and used in the methods provided herein.
  • Var. 619 4-26 Var. 482 10-34 Var. 528 16-26 Var. 574 26-34 Var. 620 4-24 Var. 483 10-32 Var. 529 16-24 Var. 575 26-32 Var. 621 4-22 Var. 484 10-30 Var. 530 16-22 Var. 576 26-30 Var. 622 4-20 Var. 485 10-28 Var. 531 16-20 Var. 577 26-28 Var. 623 4-18 Var. 486 10-26 Var. 532 16-18 Var. 578 28-40 Var. 624 4-16 Var. 487 10-24 Var. 533 18-40 Var. 579 28-38 Var. 625 4-14 Var. 488 10-22 Var. 534 18-38 Var. 580 28-36 Var. 626 4-12 Var.
  • Var. 535 18-36 Var. 581 28-34 Var. 627 4-10 Var. 490 10-18 Var. 536 18-34 Var. 582 28-32 Var. 628 4-8 Var. 491 10-16 Var. 537 18-32 Var. 583 28-30 Var. 629 6-40 Var. 492 10-14 Var. 538 18-30 Var. 584 30-40 Var. 630 6-38 Var. 493 10-12 Var. 539 18-28 Var. 585 30-38 Var. 631 6-36 Var. 494 12-40 Var. 540 18-26 Var. 586 30-36 Var. 632 6-34 Var. 495 12-38 Var. 541 18-24 Var. 587 30-34 Var. 633 6-32 Var. 496 12-36 Var. 542 18-22 Var.
  • a rVWF composition can be characterized according to the percentage of rVWF molecules that are present in a particular higher order rVWF multimer or larger multimer. For example, at least 20% of rVWF molecules in a rVWF composition used in the methods described herein are present in an oligomeric complex of at least 12 subunits.
  • a rVWF composition used in the methods provided herein has a minimal percentage (e.g., has at least X%) of rVWF molecules present in a particular higher-order rVWF multimer or larger multimer (e.g ., a multimer of at least Y subunits) according to any one of variations 134 to 457 found in Table 3 to Table 5.
  • the rVWF composition administered to the subject generally comprises a significant percentage of high molecular weight (HMW) rVWF multimers.
  • the HMW rVWF multimer composition comprises at least 40% - 80% rVWF decamers or higher order multimers.
  • the composition comprises about 40-80%, 50-75%, 60-70% decamers or higher order multimers.
  • the HMW rVWF multimer composition comprises at least about 40%, 50%, 60%, 70%, 80%, 90% decamers or higher order multimers.
  • Assessment of the number and percentage of rVWF multimers can be conducted using methods known in the art, including without limitation methods using electrophoresis and size exclusion chromatography methods to separate VWF multimers by size, for example as discussed by Cumming et al, (J Clin Pathol. 1993 May; 46(5): 470-473 ). Such techniques may further include immunoblotting techniques (such as Western Blot), in which the gel is immunoblotted with a radiolabelled antibody against VWF followed by chemiluminescent detection (see for example Wen et al., (1993), J. Clin. Lab. Anal., 7: 317-323 ).
  • immunoblotting techniques such as Western Blot
  • VWF:Antigen VWF:Ag
  • VWF:Ristocetin Cofactor VWF:RCof
  • VWF:Collagen Binding Activity assay VWF:CBA
  • higher order rVWF multimers of the invention are stable for about 1 to about 90 hours post-administration. In still further embodiments, the higher order rVWF multimers are stable for about 5-80, 10-70, 15-60, 20-50, 25-40, 30-35 hours post-administration. In yet further embodiments, the higher order rVWF multimers are stable for at least 3, 6, 12, 18, 24, 36, 48, 72 hours post-administration. In certain embodiments the stability of the rVWF multimers is assessed in vitro.
  • higher order rVWF multimers used in the compositions and methods provided herein have a half life of at least 12 hour post administration. In another embodiment, the higher order rVWF multimers have a half life of at least 24 hour post administration. In yet other embodiments, the higher order rVWF multimers have a half life selected from variations 642 to 1045 found in Table 6. Table 6. Exemplary embodiments for the half-life of higher order rVWF multimers found in the compositions and used in the methods provided herein. Hours Hours Hours Hours at least 1 Var. 642 4-22 Var. 743 14-78 Var. 844 24-30 Var. 945 at least 2 Var. 643 4-20 Var. 744 14-72 Var. 845 24-27 Var.
  • Var. 946 at least 3 Var. 644 4-18 Var. 745 14-66 Var. 846 27-90 Var. 947 at least 4 Var. 645 4-16 Var. 746 14-60 Var. 847 27-84 Var. 948 at least 5 Var. 646 4-14 Var. 747 14-54 Var. 848 27-78 Var. 949 at least 6 Var. 647 4-12 Var. 748 14-48 Var. 849 27-72 Var. 950 at least 7 Var. 648 4-10 Var. 749 14-45 Var. 850 27-66 Var. 951 at least 8 Var. 649 4-8 Var. 750 14-42 Var. 851 27-60 Var. 952 at least 9 Var. 650 4-6 Var. 751 14-39 Var. 852 27-54 Var.
  • Var. 961 at least 24 Var. 659 6-45 Var. 760 14-16 Var. 861 30-48 Var. 962 at least 27 Var. 660 6-42 Var. 761 16-90 Var. 862 30-45 Var. 963 at least 30 Var. 661 6-39 Var. 762 16-84 Var. 863 30-42 Var. 964 at least 33 Var. 662 6-36 Var. 763 16-78 Var. 864 30-39 Var. 965 at least 36 Var. 663 6-33 Var. 764 16-72 Var. 865 30-36 Var. 966 at least 39 Var. 664 6-30 Var. 765 16-66 Var. 866 30-33 Var. 967 at least 42 Var. 665 6-27 Var. 766 16-60 Var.
  • Var. 968 at least 45 Var. 666 6-24 Var. 767 16-54 Var. 868 33-84 Var. 969 at least 48 Var. 667 6-22 Var. 768 16-48 Var. 869 33-78 Var. 970 at least 54 Var. 668 6-20 Var. 769 16-45 Var. 870 33-72 Var. 971 at least 60 Var. 669 6-18 Var. 770 16-42 Var. 871 33-66 Var. 972 at least 66 Var. 670 6-16 Var. 771 16-39 Var. 872 33-60 Var. 973 at least 72 Var. 671 6-14 Var. 772 16-36 Var. 873 33-54 Var. 974 at least 78 Var. 672 6-12 Var. 773 16-33 Var.
  • Var. 975 at least 84 Var. 673 6-10 Var. 774 16-30 Var. 875 33-45 Var. 976 at least 90 Var. 674 6-8 Var. 775 16-27 Var. 876 33-42 Var. 977 2-90 Var. 675 8-90 Var. 776 16-24 Var. 877 33-29 Var. 978 2-84 Var. 676 8-84 Var. 777 16-22 Var. 878 33-36 Var. 979 2-78 Var. 677 8-78 Var. 778 16-20 Var. 879 36-90 Var. 980 2-72 Var. 678 8-72 Var. 779 16-18 Var. 880 36-84 Var. 981 2-66 Var. 679 8-66 Var. 780 18-90 Var. 881 36-78 Var.
  • Var. 991 2-27 Var. 689 8-27 Var. 790 18-39 Var. 891 39-84 Var. 992 2-24 Var. 690 8-24 Var. 791 18-36 Var. 892 39-78 Var. 993 2-22 Var. 691 8-22 Var. 792 18-33 Var. 893 39-72 Var. 994 2-20 Var. 692 8-20 Var. 793 18-30 Var. 894 39-66 Var. 995 2-18 Var. 693 8-18 Var. 794 18-27 Var. 895 39-60 Var. 996 2-16 Var. 694 8-16 Var.
  • Var. 896 39-54 Var. 997 2-14 Var. 695 8-14 Var. 796 18-22 Var. 897 39-48 Var. 998 2-12 Var. 696 8-12 Var. 797 18-20 Var. 898 39-45 Var. 999 2-10 Var. 697 8-10 Var. 798 20-90 Var. 899 39-42 Var. 1 000 2-8 Var. 698 10-90 Var. 799 20-84 Var. 900 42-90 Var. 1001 2-6 Var. 699 10-84 Var. 800 20-78 Var. 901 42-84 Var. 1002 2-4 Var. 700 10-78 Var. 801 20-72 Var. 902 42-78 Var. 1003 3-90 Var. 701 10-72 Var. 802 20-66 Var. 903 42-72 Var.
  • rVWF of use in the present invention increases stability of plasma FVIII, which, as will be appreciated, may include pdFVII or rFVIII which has been administered to the patient or it may include FVIII endogenous to the patient, or any combination thereof.
  • plasma FVIII may include pdFVII or rFVIII which has been administered to the patient or it may include FVIII endogenous to the patient, or any combination thereof.
  • the half-life of plasma FVIII is increased in VWD patients receiving rVWF in combination with rFVIII as compared to patients receiving FVIII (i.e., Advate) alone.
  • rVWF increases half-life of E'VIII by about 1.5 - 5-fold as compared to the half-life seen with patients receiving FVIII alone.
  • rVWF increases half-life of FVIII by about 1.0 - 4.5, 1.5 - 4.0, 2.0 - 3.5, 2.5 - 3.0 fold.
  • administration of rVWF increases the stability of plasma FVIII, as compared to the administration of plasma-derived VWF, by an amount selected from variations 1046 to 1089 found in Table 7.
  • administration of a rVWF/FVIII complex increases the stability of plasma FVIII, as compared to the administration of plasma-derived VWF, by an amount selected from variations 1046 to 1089 found in Table 7. Table 7.
  • Exemplary embodiments for the increase in half-life experienced by plasma FVIII after administration of rVWF and rVWF/FVIII complexes as compared to after administration of plasma-derived VWF and plasma-derived VWF/FVIII complexes.
  • Increase in plasma FVIII half-life Increase in plasma FVIII half-life Increase in plasma FVIII half-life Increase in plasma FVIII half-life Increase in plasma FVIII half-life at least 1.5-fold Var. 1046 3.0-fold Var. 1057 1.5-2.0 fold Var. 1068 2.5-3.0 fold Var. 1079 at least 2.0-fold Var. 1047 3.5-fold Var. 1058 2-5.0 fold Var. 1069 3-5.0 fold Var. 1080 at least 2.5-fold Var. 1048 4.0-fold Var. 1059 2-4.5 fold Var.
  • the increase in FVIII half-life is maintained at least 10, 20, 30, 40, 50, 60, 70, 80, 90, 100 hours after administration of rVWF. In yet further embodiments, the increase in FVIII half-life is maintained at least 5-125, 10-115, 15-105, 20-95, 25-85, 30-75, 35-65, 40-55 hours after administration of rVWF.
  • the increase in the mean residence time (MRT) plasma FVIII is maintained for a time selected from variations 1090 to 1299 found in Table 8, after administration of rVWF.
  • the increase in the half life of plasma FVIII is maintained for a time selected from variations 1090 to 1299 found in Table 8, after administration of a rVWF/FVIII complex.
  • Table 8 Exemplary embodiments for the time plasma FVIII stability is maintained after administration of rVWF and rVWF/FVIII complexes. Hours Hours Hours Hours at least 6 Var. 1090 12-36 Var. 1143 36-114 Var. 1196 60-102 Var. 1248 at least 12 Var. 1091 12-30 Var. 1144 36-1.08 Var.
  • Var. 1262 at least 96 Var. 1105 18-54 Var. 1158 42-108 Var. 1211 66-72.
  • Var. 1263 at least 102 Var. 1106 18-48 Var. 1159 42-102 Var. 1212 72-120 Var. 1264 at least 108 Var. 1107 18-42 Var. 1160 42-96 Var. 1213 72-114 Var. 1265 at least 114 Var. 1108 18-36 Var. 1161 42-90 Var. 1214 72-108 Var. 1266 at least 120 Var. 1109 18-30 Var. 1162 42-84 Var. 1215 72-102 Var. 1267 6-120 Var. 1110 18-24 Var. 1163 42-78 Var. 1216 72-96 Var. 1268 6-114 Var. 1111 24-120 Var. 1164 42-72 Var.
  • the rVWF of the invention shows an increased effect on the stability of FVIII as compared to the effect of pdVWF.
  • average FVIII half-life was increased by rVWF by 5.2 hours over the half-life for patients receiving pdVWF.
  • rVWF increases average FVIII half-life by about 1-15, 2-14, 3-13, 4-12, 5-11, 6-10, 5-9, 6-8 hours.
  • rVWF increases FVIII half-life by about 10% to about 75% as compared to pdVWF.
  • rVWF increases FVIII half-life by about 10-80%, 15-65%, 20-60%, 25-55%, 30-50%, 35-45% as compared to pdVWF.
  • the administration of rVWF increases the half life of FVIII by an amount selected from variations 1300 to 1643 found in Table 9 , as compared to administration of plasma-derived VWF.
  • the average or percentage increase in FVIII half-life is maintained at least 10, 20, 30, 40, 50, 60, 70, 80, 90, 100 hours after administration of rVWF.
  • the increase in FVIII half-life is maintained at least 5-125, 10-115, 15-105, 20-95, 25-85, 30-75, 35-65, 40-55 hours after administration of rVWF.
  • Table 9 Exemplary embodiments for the increase in half-life experienced by plasma FVIII after administration of rVWF and rVWF/FVIII complexes. Increase in half life Increase in half life Increase in half life Increase in half life at least 1 hr Var. 1300 5-8 hr Var. 1387 10-95% Var. 1474 35-60% Var. 1561 at least 2 hr Var. 1301 5-7 hr Var. 1388 10-90% Var. 1475 35-55% Var. 1562 at least 3 hr Var.
  • Var. 1389 10-85% Var. 1476 35-50% Var. 1563 at least 4 hr Var. 1303 6-15 hr Var. 1390 10-80% Var. 1477 35-45% Var. 1564 at least 5 hr Var. 1304 6-14 hr Var. 1391 10-75% Var. 1478 35-40% Var. 1565 at least 6 hr Var. 1305 6-13 hr Var. 1392 1 0-70% Var. 1479 40-100% Var. 1566 at least 7 hr Var. 1306 6-12 hr Var. 1393 10-65% Var. 1480 40-95% Var. 1567 at least 8 hr Var. 1307 6-11 hr Var. 1394 10-60% Var. 1481 40-90% Var.
  • Var. 1568 at least 9 hr Var. 1308 6-10 hr Var. 1395 10-55% Var. 1482 40-85% Var. 1569 at least 10 hr Var. 1309 6-9 hr Var. 1396 10-50% Var. 1483 40-80% Var. 1570 at least 11 hr Var. 1310 6-8 hr Var. 1397 10-45% Var. 1484 40-75% Var. 1571 at least 12 hr Var. 1311 6-7 hr Var. 1398 10-40% Var. 1485 40-70% Var. 1572 at least 13 hr Var. 1312 7-15 hr Var. 1399 10-35% Var. 1486 40-65% Var. 1573 at least 14 hr Var. 1313 7-14 hr Var. 1400 10-30% Var.
  • Var. 1505 50-85% Var. 1592 1-13 hr Var. 1332 9-10 hr Var. 1419 15-25% Var. 1506 50-80% Var. 1593 1-12 hr Var. 1333 10-15 hr Var. 1420 15-20% Var. 1507 50-75% Var. 1594 1-11 hr Var. 1334 10-14 hr Var. 1421 20-100% Var. 1508 50-70% Var. 1595 1-10 hr Var. 1335 10-13 hr Var. 1422 20-95% Var. 1509 50-65% Var. 1596 1-9 hr Var. 1336 10-12 hr Var. 1423 20-90% Var. 1510 50-60% Var. 1597 1-8 hr Var. 1337 10-11 hr Var. 1424 20-85% Var.
  • Var. 1610 2-9 hr Var. 1350 at least 20% Var. 1437 25-100% Var. 1524 60-85% Var. 1611 2-8 hr Var. 1351 at least 25% Var. 1438 25-95% Var. 1525 60-80% Var. 1612 2-7 hr Var. 1352 at least 30% Var. 1439 25-90% Var. 1526 60-75% Var. 1613 2-6 hr Var. 1353 at least 35% Var. 1440 25-85% Var. 1527 60-70% Var. 1614 2-5 hr Var. 1354 at least 40% Var. 1441 25-80% Var. 1528 60-65% Var. 1615 2-4 hr Var. 1355 at least 45% Var. 1442 25-75% Var. 1529 65-100% Var.
  • Var. 1356 at least 50% Var. 1443 25-70% Var. 1530 65-95% Var. 1617 3-15 hr Var. 1357 at least 55% Var. 1444 25-65% Var. 1531 65-90% Var. 1618 3-14 hr Var. 1358 at least 60% Var. 1445 25-60% Var. 1532 65-85% Var. 1619 3-13 hr Var. 1359 at least 65% Var. 1446 25-55% Var. 1533 65-80% Var. 1620 3-12 hr Var. 1360 at least 70% Var. 1447 25-50% Var. 1534 65-75% Var. 1621 3-11 hr Var. 1361 at least 75% Var. 1448 25-45% Var. 1535 65-70% Var. 1622 3-10 hr Var.
  • Var. 1362 at least 80% Var. 1449 25-40% Var. 1536 70-100% Var. 1623 3-9 hr Var. 1363 at least 85% Var. 1450 25-35% Var. 1537 70-95% Var. 1624 4 3-8 hr Var. 1364 at least 90% Var. 1451 25-30% Var. 1538 70-90% Var. 1625 3-7 hr Var. 1365 at least 95% Var. 1452 30-100% Var. 1539 70-85% Var. 1626 3-6 hr Var. 1366 at least 100% Var. 1453 30-95% Var. 1540 70-80% Var. 1627 3-5 hr Var. 1367 10% Var. 1454 30-90% Var. 1541 70-75% Var. 1628 3-4 hr Var. 1368 15% Var.
  • Var. 1455 30-85% Var. 1542 75-100% Var. 1629 4-15 hr Var. 1369 20% Var. 1456 30-80% Var. 1543 75-95% Var. 1630 4-14 hr Var. 1370 25% Var. 1457 30-75% Var. 1544 75-90% Var. 1631 4-13 hr Var. 1371 30% Var. 1458 30-70% Var. 1545 75-85% Var. 1632 4-12 br Var. 1372 35% Var. 1459 30-65% Var. 1546 75-80% Var. 1633 4-11 hr Var. 1373 40% Var. 1460 30-60% Var. 1547 80-100% Var. 1634 4-10 hr Var. 1374 45% Var. 1461 30-55% Var. 1548 80-95% Var. 1635 4-9 hr Var.
  • Var. 1462 30-50% Var. 1549 80-90% Var. 1636 4-8 hr Var. 1376 55% Var. 1463 30-45% Var. 1550 80-85% Var. 1637 4-7 hr Var. 1377 60% Var. 1464 30-40% Var. 1551 85-100% Var. 1638 4-6 hr Var. 1378 65% Var. 1465 30-35% Var. 1552 85-95% Var. 1639 4-5 hr Var. 1379 70% Var. 1 466 35-100% Var. 1553 85-90% Var. 1640 5-15 hr Var. 1380 75% Var. 1467 35-95% Var. 1554 90-100% Var. 1641 5-14 hr Var. 1381 80% Var. 1468 35-90% Var. 1555 90-95% Var.
  • Var. Variation
  • the stabilization of FVIII activity by rVWF as compared to pdVWF can be measured by metrics in addition to FVIII half-life, including mean residence time (MRT) and area under curve (AUC).
  • MRT mean residence time
  • AUC area under curve
  • rVWF increases MRT by about 1-15 hours as compared to pdVWF.
  • rVWF increases MRT by about 1-25, 2-20, 3-15, 4-10, 5-9, 6-8 hours as compared to pdVWF.
  • rVWF increases FVIII MRT by about 10-80%, 15-65%, 20-60%, 25-55%, 30-50%, 35-45% as compared to pdVWF.
  • the average or percentage increase in FVIII half-life is maintained at least 10, 20, 30, 40, 50, 60, 70, 80, 90, 100 hours after administration of rVWF.
  • the administration of rVWF increases the MRT of FVIII by an amount selected from variations 1644 to 1987 found in Table 10, as compared to administration of plasma-derived VWF.
  • the increase in MRT is maintained at least 5-125, 10-115, 15-105, 20-95, 25-85, 30-75, 35-65, 40-55 hours after administration of rVWF.
  • the increase in MRT of FVIII caused by administration of rVWF is maintained for a time selected from variations 1090 to 1299 found in Table 8.
  • Table 10 Exemplary embodiments for the increase in FVIII mean residence time after administration of rVWF and rVWF/FVIII complexes, as compared to after administration of plasma-derived VWF and plasma-derived VWF/FVIII complexes.
  • Increase in half life Increase in half life Increase in half life Increase in half life at least 1 hr Var. 1644 5-9 hr Var.
  • Var. 1730 100% Var. 1816 35-75% Var. 1902 at least 2 hr Var. 1645 5-8 hr Var. 1731 10-100% Var. 1817 35-70% Var. 1903 at least 3 hr Var. 1 646 5-7 hr Var. 1732 10-95% Var. 1818 35-65% Var. 1904 at least 4 hr Var. 1647 5-6 hr Var. 1733 10-90% Var. 1819 35-60% Var. 1905 at least 5 hr Var. 1648 6-15 hr Var. 1734 10-85% Var. 1820 35-55% Var. 1906 at least 6 hr Var. 1649 6-14 hr Var. 1735 10-80% Var. 1821 35-50% Var. 1907 at least 7 hr Var.
  • Var. 1760 15-45% Var. 1846 45-50% Var. 1932 1- 14 hr Var. 1675 9-12 hr Var. 1761 15-40% Var. 1847 50-100% Var. 1933 1-13 hr Var. 1676 9-11 hr Var. 1762 15-35% Var. 1848 50-95% Var. 1934 1-12 hr Var. 1677 9-10 hr Var. 1763 15-30% Var. 1849 50-90% Var. 193 5 1-11 hr Var. 1678 10-15 hr Var. 1764 15-25% Var. 1850 50-85% Var. 1936 1-10 hr Var. 1679 10-14 hr Var. 1765 15-20% Var. 1851 50-80% Var. 1937 1-9 hr Var.
  • Var. 1680 10-13 hr Var. 1766 20-100% Var. 1852 50-75% Var. 1938 1-8 hr Var. 1681 10-12 hr Var. 1767 20-95% Var. 1853 50-70% Var. 1939 1-7 hr Var. 1682 10-11 hr Var. 1768 20-90% Var. 1854 50-65% Var. 1940 1-6 hr Var. 1683 11-15 hr Var. 1769 20-85% Var. 1855 50-60% Var. 1941 1-5 hr Var. 1684 11-14 hr Var. 1770 20-80% Var. 1856 50-55% Var. 1942 1-4 hr Var. 1685 11-13 hr Var. 1771 20-75% Var. 1857 55-100% Var. 1943 1-3 hr Var.
  • Var. 1778 14-15 hr Var. 1778 20-40% Var. 1864 55-65% Var. 1950 2-10 hr Var. 1693 at least 10% Var. 1779 20-35% Var. 1865 55-60% Var. 1951 2-9 hr Var. 1694 at least 15% Var. 1780 20-30% Var. 1866 60-100% Var. 1952 2-8 hr Var. 1695 at least 20% Var. 1781 20-25% Var. 1867 60-95% Var. 1953 2-7 hr Var. 1696 at least 25% Var. 1782 25-100% Var. 1868 60-90% Var. 1954 2-6 hr Var. 1697 at least 30% Var. 1783 25-95% Var. 1869 60-85% Var. 1955 2-5 hr Var. 1698 at least 35% Var. 1784 25-90% Var.
  • Var. 1705 at least 70% Var. 1791 25-55% Var. 1877 65-85% Var. 1963 3-10 hr Var. 1706 at least 75% Var. 1792 25-50% Var. 1878 65-80% Var. 1964 3-9 hr Var. 1707 at least 80% Var. 1793 25-45% Var. 1879 65-75% Var. 1965 3-8 hr Var. 1708 at least 85% Var. 1794 25-40% Var. 1880 65-70% Var. 1966 3-7 hr Var. 1709 at least 90% Var. 1795 25-35% Var. 1881 70-100% Var. 1967 3-6 hr Var. 1710 at least 95% Var. 1796 25-30% Var. 1882 70-95% Var. 1968 3-5 hr Var. 1711 at least 100% Var. 1797 30-100% Var.
  • Var. 1964 3-4 hr Var. 1712 10% Var. 1798 30-95% Var. 1 884 70-85% Var. 1970 4-15 hr Var. 1713 15% Var. 1799 30-90% Var. 1885 70-80% Var. 1971 4-14 hr Var. 1714 20% Var. 1800 30-85% Var. 1886 70-75% Var. 1972 4-13 hr Var. 1715 25% Var. 1801 30-80% Var. 1887 75-100% Var. 1973 4-12 hr Var. 1716 30% Var. 1802 30-75% Var. 1888 75-95% Var. 1974 4-11 hr Var. 1717 35% Var. 1803 30-70% Var. 1889 75-90% Var. 1975 4-10 hr Var. 1718 40% Var. 1804 30-65% Var.
  • pdVWF rVWF Synthesized in endothelial cells and megakaryocytes ā€¢ Expressed in CHO cells ā€¢ Post-translational modification of propeptide removal occurs intracellularly: during passage of the protein to the Golgi and post-Golgi compartments ā€¢ Propeptide removal mediated in vitro through exposure of the pro-VWF to recombinant Furin ā€¢ Glycosylation / ABO blood group glycans present ā€¢ Fully glycosylated / ABO blood group gylcans absent ā€¢ Consists of VWF subunits that have been exposed to plasma ADAMTS13 ā€¢ No exposure to ADAMTS13 ā‡ Ultra-large VWF multimers absent ā‡ Intact VWF subunits ā‡ Subunits cleaved at TYR 1605 -MET 1606 ā‡ Ultra-large VWF multimers present ā‡ Subunit cleavage occurs upon ADAMTS
  • the ratio of rFVIII procoagulant activity (IU rFVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) is between 3:1 and 1:5. In further embodiments, the ratio is between 2:1 and 1:4. In still further embodiments, the ratio is between 5:2 and 1:4. In further embodiments, the ratio is between 3:2 and 1:3. In still further embodiments, the ratio is about 1:1, 1:2, 1:3, 1:4, 1:5, 2:1, 2:3, 2:4, 2:5, 3:1, 3:2, 3:4, or 3:5. In further embodiments, the ratio is between 1:1 and 1:2.
  • the ratio is 1.1:1, 1.2:1, 1.3:1, 1.4:1, 1.5:1, 1.6:1, 1.7:1, 1.8:1, 1.9:1, or 2:1.
  • the ratio of rFVIII procoagulant activity (IU rFVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) in a composition useful for a method described herein is selected from variations 1988 to 2140 found in Table 11. Table 11.
  • the rVWF and/or the FVIII (recombinant or plasma derived) used in accordance with the present invention are not modified with any conjugation, post-translation or covalent modifications.
  • the rVWF and/or FVIII of the present invention are not modified with a water soluble polymer, including without limitation, a polyethylene glycol (PEG), a polypropylene glycol, a polyoxyalkylene, a polysialic acid, hydroxyl ethyl starch, a poly-carbohydrate moiety, and the like.
  • the rVWF and/or the FVIII (recombinant or plasma derived) used in accordance with the present invention are modified through conjugation, post-translation modification, or covalent modification, including modifications of the N- or C- terminal residues as well as modifications of selected side chains, for example, at free sulfhydryl-groups, primary amines, and hydroxyl-groups.
  • a water soluble polymer is linked to the protein (directly or via a linker) by a lysine group or other primary amine.
  • the rVWF and/or FVIII proteins of the present invention may be modified by conjugation of a water soluble polymer, including without limitation, a polyethylene glycol (PEG), a polypropylene glycol, a polyoxyalkylene, a polysialic acid, hydroxyl ethyl starch, a poly-carbohydrate moiety, and the like.
  • a water soluble polymer including without limitation, a polyethylene glycol (PEG), a polypropylene glycol, a polyoxyalkylene, a polysialic acid, hydroxyl ethyl starch, a poly-carbohydrate moiety, and the like.
  • Water soluble polymers that may be used to modify the rVWF and/or FVIII include linear and branched structures.
  • the conjugated polymers may be attached directly to the coagulation proteins of the invention, or alternatively may be attached through a linking moiety.
  • Non-limiting examples of protein conjugation with water soluble polymers can be found in U.S. Patent Nos. 4,640,835 ; 4,496,689 ; 4,301,144 ; 4,670,417 ; 4,791,192 , and 4,179,337 , as well as in Abuchowski and Davis "Enzymes as Drugs," Holcenberg and Roberts, Eds., pp. 367 383, John Wiley and Sons, New York (1981 ), and Hermanson G., Bioconjugate Techniques 2nd Ed., Academic Press, Inc. 2008 .
  • Protein conjugation may be performed by a number of well known techniques in the art, for example, see Hermanson G., Bioconjugate Techniques 2nd Ed., Academic Press, Inc. 2008 . Examples include linkage through the peptide bond between a carboxyl group on one of either the coagulation protein or water-soluble polymer moiety and an amine group of the other, or an ester linkage between a carboxyl group of one and a hydroxyl group of the other.
  • a coagulation protein of the invention could be conjugated to a water-soluble polymer compound
  • a Schiff base between a free amino group on the polymer moiety being reacted with an aldehyde group formed at the non-reducing end of the polymer by periodate oxidation ( Jennings and Lugowski, J. Immunol. 1981; 127:1011-8 ; Femandes and Gregonradis, Biochim Biophys Acta. 1997; 1341; 26-34 ).
  • the generated Schiff Base can be stabilized by specific reduction with NaCNBH 3 to form a secondary amine.
  • An alternative approach is the generation of terminal free amino groups on the polymer by reductive amination with NH 4 Cl after prior oxidation.
  • Bifunctional reagents can be used for linking two amino or two hydroxyl groups.
  • a polymer containing an amino group can be coupled to an amino group of the coagulation protein with reagents like BS3 (Bis(sulfosuccinimidyl)suberate/Pierce, Rockford, Ill.).
  • reagents like BS3 (Bis(sulfosuccinimidyl)suberate/Pierce, Rockford, Ill.).
  • heterobifunctional cross linking reagents like Sulfo-EMCS (N- ā‡ -Maleimidocaproyloxy)sulfosuccinimide ester/Pierce) can be used for instance to link amine and thiol groups.
  • an aldehyde reactive group such as PEG alkoxide plus diethyl acetal of bromoacetaldehyde; PEG plus DMSO and acetic anhydride, and PEG chloride plus the phenoxide of 4-hydroxybenzaldehyde, succinimidyl active esters, activated dithiocarbonate PEG, 2,4,5-trichlorophenylcloroformate and P-nitrophenylcloro activated PEG, may be used in the conjugation of a coagulation protein.
  • the rVWF used in methods of the present invention has been matured in vitro with Furin.
  • the Furin is recombinant Furin.
  • the rVWF and/or rFVIII used in the methods of the present invention are produced by expression in a mammalian cell culture using methods known in the art.
  • the mammalian culture comprises CHO cells.
  • the rVWF and the rFVIII are co-expressed in the same culture.
  • the rVWF and the rFVIII are purified together (co-purified) or separately using methods known in the art.
  • the rV WF and the rFVIII are expressed in different cultures.
  • the rVWF of the invention comprises rVWF protein isolated from a CHO cell expression system.
  • the propeptide removal is mediated in vitro through exposure of the pro-VWF to Furin - in a still further embodiment, the Furin used for propeptide removal is recombinant Furin.
  • fully glycosylated/ABO blood group glycans are absent.
  • the rVWF used in methods and compositions of the present invention by expression in a suitable eukaryotic host system.
  • eukaryotic cells include, without limitation, mammalian cells, such as CHO, COS, HEK 293, BHK, SK-Hep, and HepG2; insect cells, e.g., SF9 cells, SF21 cells, S2 cells, and High Five cells; and yeast cells, e.g., Saccharomyces or Schizosaccharomyces cells.
  • the VWF can be expressed in yeast cells, insect cells, avian cells, mammalian cells, and the like.
  • the cell line is a CHO, BHK, or HEK cell line.
  • mammalian cells e.g., CHO cell from a continuous cell line, can be used to express the VWF of the present invention.
  • the nucleic acid sequence comprising a sequence coding for VWF can be a vector.
  • the vector can be delivered by a virus or can be a plasmid.
  • the nucleic acid sequence coding for the protein can be a specific gene or a biologically functional part thereof.
  • the protein is at least a biologically active part of VWF.
  • vectors can be used for the expression of the VWF and can be selected from eukaryotic expression vectors.
  • examples of vectors for eukaryotic expression include: (i) for expression in yeast, vectors such as pAO, pPIC, pYES, pMET, using promoters such as AOX1, GAP, GAL1, AUG1, etc; (ii) for expression in insect cells, vectors such as pMT, pAc5, pIB, pMIB, pBAC, etc., using promoters such as PH, p10, MT, Ac5, OpIE2, gp64, polh, etc., and (iii) for expression in mammalian cells, vectors such as pSVL, pCMV, pRc/RSV, pcDNA3, pBPV, etc., and vectors derived from viral systems such as vaccinia vims, adeno-associated viruses, herpes viruses, retroviruses, etc.
  • the nucleic acid sequence further comprises other sequences suitable for a controlled expression of a protein such as promoter sequences, enhancers, TATA boxes, transcription initiation sites, polylinkers, restriction sites, poly-A-sequences, protein processing sequences, selection markers, and the like which are generally known to a person of ordinary skill in the art.
  • the cell-culture methods of the invention may comprise the use of a microcarrier.
  • the cell-cultures of the embodiments can be performed in large bioreactors under conditions suitable for providing high volume-specific culture surface areas to achieve high cell densities and protein expression.
  • One means for providing such growth conditions is to use microcarriers for cell-culture in stirred tank bioreactors.
  • the concept of cell-growth on microcarriers was first described by van Wezel ( van Wezel, A.L., Nature 216:64-5 (1967 )) and allows for cell attachment on the surface of small solid particles suspended in the growth medium. These methods provide for high surface-to-volume ratios and thus allow for efficient nutrient utilization.
  • the cells expressing VWF can be bound to a spherical or a porous microcarrier during cell culture growth.
  • the microcarrier can be a microcarrier selected from the group of microcarriers based on dextran, collagen, plastic, gelatine and cellulose and others as described in Butler (1988. In: Spier & Griffiths, Animal Cell Biotechnology 3:283-303 ). It is also possible to grow the cells to a biomass on spherical microcarriers and subculture the cells when they have reached final fermenter biomass and prior to production of the expressed protein on a porous microcarrier or vice versa.
  • Suitable spherical microcarriers can include smooth surface microcarriers, such as CytodexTM 1, CytodexTM 2, and CytodexTM 3 (GE Healthcare) and macroporous microcarriers such as CytoporeTM 1, CytoporeTM 2, CytolineTM 1, and CytolineTM 2 (GE Healthcare).
  • smooth surface microcarriers such as CytodexTM 1, CytodexTM 2, and CytodexTM 3 (GE Healthcare) and macroporous microcarriers such as CytoporeTM 1, CytoporeTM 2, CytolineTM 1, and CytolineTM 2 (GE Healthcare).
  • rVWF is expressed in cells cultured in cell culture media that produces high molecular weight rVWF.
  • cell culture solution can include cell culture media and cell culture supernatant.
  • the cell culture media are externally added to the cell culture solution, optionally together with supplements, to provide nutrients and other components for culturing the cells expressing VWF.
  • the cell culture supernatant refers to a cell culture solution comprising the nutrients and other components from the cell culture medium as well as products released, metabolized, and/or excreted from the cells during culture.
  • the media can be animal protein-free and chemically defined.
  • Methods of preparing animal protein-free and chemically defined culture media are known in the art, for example in US 2008/0009040 and US 2007/0212770 , which are both incorporated herein for all purposes and in particular for all teachings related to cell culture media.
  • Protein free and related terms refers to protein that is from a source exogenous to or other than the cells in the culture, which naturally shed proteins during growth.
  • the culture medium is polypeptide free.
  • the culture medium is serum free.
  • the culture medium is animal protein free.
  • the culture medium is animal component free.
  • the culture medium contains protein, e.g., animal protein from serum such as fetal calf serum.
  • the culture has recombinant proteins exogenously added.
  • the proteins are from a certified pathogen free animal.
  • the term "chemically definedā€ as used herein shall mean, that the medium does not comprise any undefined supplements, such as, for example, extracts of animal components, organs, glands, plants, or yeast. Accordingly, each component of a chemically defined medium is accurately defined.
  • the media are animal-component free and protein free.
  • the culture of cells expressing VWF can be maintained for at least about 7 days, or at least about 14 days, 21 days, 28 days, or at least about 5 weeks, 6 weeks, 7 weeks, or at least about 2 months, or 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18 months or longer.
  • the cell density at which a cell-culture is maintained at for production of a recombinant VWF protein will depend upon the culture-conditions and medium used for protein expression. One of skill in the art will readily be able to determine the optimal cell density for a cell-culture producing an VWF.
  • the culture is maintained at a cell density of between about 0.5x10 6 and 4x10 7 cells/ml for an extended period of time.
  • the cell density is maintained at a concentration of between about 1,0x10 6 and about 1.0x10 7 cells/ml for an extended period of time. In other embodiments, the cell density is maintained at a concentration of between about 1.0x10 6 and about 4.0x10 6 cells/ml for an extended period of time. In other embodiments, the cell density is maintained at a concentration of between about 1.0x10 6 and about 4.0x10 6 cells/ml for an extended period of time.
  • the cell density may be maintained at a concentration between about 2.0x10 6 and about 4.0x10 6 , or between about 1.0x10 6 and about 2.5x10 6 , or between about 1.5x10 6 and about 3.5x10 6 , or any other similar range, for an extended period of time.
  • the rVWF can be isolated from the expression system using methods known in the art.
  • the cell density of the continuous cell culture for production of rVWF is maintained at a concentration of no more than 2.5x10 6 cells/mL for an extended period. In other specific embodiments, the cell density is maintained at no more than 2.0x10 6 cells/mL, 1.5x10 6 cells/mL, 1.0x10 6 cells/mL, 0.5x10 6 cells/mL, or less. In one embodiment, the cell density is maintained at between 1.5x10 6 cells/mL and 2.5x10 6 cells/mL.
  • the cell culture solution comprises a medium supplement comprising copper.
  • a medium supplement comprising copper.
  • the rFVIII/rVWF complex is reconstituted prior to administration.
  • the rVWF is treated with Furin prior to or subsequent to reconstitution of the rFVIII/rVWF complex.
  • the Furin is recombinant Furin.
  • the rVWF of the invention is not exposed to ADAMTS13, with the result that ultra large (i.e., comprising 10 or more subunits) are present in rVWF compositions of the invention.
  • the rVWF and/or the rFVIII used in methods of the present invention are contained in a formulation containing a buffer, a sugar and/or a sugar alcohol (including without limitation trehalose and mannitol), a stabilizer (such as glycine), and a surfactant (such as Polysorbate 80).
  • the formulation may further include sodium, histidine, calcium, and glutathione.
  • the formulations comprising rVWF and/or rFVIII are lyophilized prior to administration. Lyophilization is carried out using techniques common in the art and should be optimized for the composition being developed [ Tang et al., Pharm Res. 21:191-200, (2004 ) and Chang et al., Pharm Res. 13:243-9 (1996 )].
  • Methods of preparing pharmaceutical formulations can include one or more of the following steps: adding a stabilizing agent as described herein to said mixture prior to lyophilizing, adding at least one agent selected from a bulking agent, an osmolarity regulating agent, and a surfactant, each of which as described herein, to said mixture prior to lyophilization.
  • a lyophilized formulation is, in one aspect, at least comprised of one or more of a buffer, a bulking agent, and a stabilizer.
  • the utility of a surfactant is evaluated and selected in cases where aggregation during the lyophilization step or during reconstitution becomes an issue.
  • An appropriate buffering agent is included to maintain the formulation within stable zones of pH during lyophilization.
  • the lyophilized material may be reconstituted as an aqueous solution.
  • aqueous carriers e.g., sterile water for injection, water with preservatives for multi dose use, or water with appropriate amounts of surfactants (for example, an aqueous suspension that contains the active compound in admixture with excipients suitable for the manufacture of aqueous suspensions).
  • excipients are suspending agents, for example and without limitation, sodium carboxymethylcellulose, methylcellulose, hydroxypropylmethylcellulose, sodium alginate, polyvinylpyrrolidone, gum tragacanth and gum acacia; dispersing or wetting agents are a naturally-occurring phosphatide, for example and without limitation, lecithin, or condensation products of an alkylene oxide with fatty acids, for example and without limitation, polyoxyethylene stearate, or condensation products of ethylene oxide with long chain aliphatic alcohols, for example and without limitation, heptadeeaethyl-eneoxycetanol, or condensation products of ethylene oxide with partial esters derived from fatty acids and a hexitol such as polyoxyethylene sorbitol monooleate, or condensation products of ethylene oxide with partial esters derived from fatty acids and hexitol anhydrides, for example and without limitation, polyethylene sorbitan monooleate.
  • compositions of the present invention are liquid formulations for administration with the use of a syringe or other storage vessel.
  • these liquid formulations are produced from lyophilized material described herein reconstituted as an aqueous solution.
  • compositions of the invention further comprise one or more pharmaceutically acceptable carriers.
  • pharmaceutically acceptable carriers include any and all clinically useful solvents, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absorption delaying agents and the like, including those agents disclosed above.
  • compositions of the invention for methods of treating disease
  • rVWF compositions provide the further flexibility of re-dosing with rVWF alone after an initial co-administration of rVWF and FVIII, without need for additional dosing with FVIII.
  • the co-administered FVIII may be recombinant or plasma derived.
  • the administration of rVWF in accordance with the invention results in higher plasma FVIII levels and/or activity in the subject than is seen with a subject administered pdVWF.
  • increases in FVIII levels and activity can be measured using methods standard in the art, thus allowing for determination of appropriate dosages for rVWF with or without FVIII.
  • Single or multiple administrations of rVWF are carried out with the dose levels and pattern being selected by the treating physician.
  • the appropriate dosage depends on the type of disease to be treated (e.g., von Willebrand disease), the severity and course of the disease, whether drug is administered for preventive or therapeutic purposes, previous therapy, the patient's clinical history and response to the drug, and the discretion of the attending physician.
  • treatment of VWD may involve an initial treatment of rVWF alone or in combination with FVIII, followed by one or more repeat doses of rVWF alone, rVWF plus FVIII together, or FVIII alone.
  • the nature of the initial and then the subsequent repeat administrations will depend in part on the disease being treated. For example, patients with VWD have some level of FVIII, but the stability of that FVIII is generally compromised because these patients lack VWF.
  • Treatment of VWD patients may thus in some embodiments involve an initial treatment with both rVWF and rFVIII followed by repeated administrations of rVWF alone.
  • the initial treatment may be with rVWF alone while subsequent repeated administrations are with both rVWF and rFVIII.
  • the initial and subsequent repeat administrations may all include a co-administration of both rVWF and rFVIII.
  • the initial treatment may be rFVIII alone while the subsequent repeat treatments involve co-administration of rVWF and rFVIII.
  • rVWF is administered to a subject in doses ranging from 0.5 IU/kg - 200 IU/kg, In some embodiments, rVWF is administered in doses ranging from 1-190, 5-180, 10-170, 15-160, 20-150, 25-140, 30-130, 35-120, 40-110, 45-100, 50-90, 55-80, or 60-70 IU/kg. In further embodiments and in accordance with any of the above , rVWF (with or without FVIII) is administered to a subject at doses of between about 1 IU/kg to about 150 IU/kg rVWF.
  • the rVWF and rFVIII is administered at doses of between 1.5 IU/kg to 150 IU/kg, 2 IU/kg to 50 IU/kg, 5 IU/kg to 40 IU/kg, 10 IU/kg to 20 IU/kg, 10 IU/kg to 100 IU/kg, 25 IU/kg to 75 IU/kg, and 40 IU/kg to 75 IU/kg.
  • rVWF is administered at 2, 5, 7.5, 10, 15, 20, 25, 30, 35, 40, 45, or 50 IU/kg.
  • rVWF is administered to a subject in a dose selected from variations 2141 to 2338 in Table 12. Table 12. Exemplary embodiments for the dosage of rVWF administered to a subject according to the methods provided herein. IU/kg IU/kg IU/kg About 0.5 Var. 2141 0.5-75 Var. 2191 5-40 Var. 2241 20-50 Var. 2290 About 1 Var. 2142 0.5-50 Var. 2192 5-30 Var. 2242 20-40 Var.
  • Var. 2150 0.5-5 Var. 2200 7.5-150 Var. 2250 25-75 Var. 2299 About 30 Var. 2151 0.5-2.5 Var. 2201 7.5-125 Var. 2251 25-50 Var. 2300 About 35 Var. 2152 0.5-1 Var. 2202 7.5-100 Var. 2252 25-40 Var. 2301 About 40 Var. 2153 1-200 Var. 2203 7.5-75 Var. 2253 25-30 Var. 2302 About 45 Var. 2154 1-175 Var. 2204 7.5-50 Var. 2254 30-200 Var. 2303 About 50 Var. 2155 1-150 Var. 2205 7.5-40 Var. 2255 30-175 Var. 2304 About 55 Var. 2156 1-125 Var. 2206 7.5-30 Var. 2256 30-150 Var. 2305 About 60 Var. 2157 1-100 Var.
  • rVWF is administered at a dose such that it increases half-life of plasma FVIII by about 1.0 - 4.5, 1.5 - 4.0, 2.0 - 3.5, 2.5 - 3.0 fold.
  • the dose and/or frequency of rVWF administration is such that the increase in FVIII half-life is maintained at least 10, 20, 30, 40, 50, 60, 70, 80, 90, 100 hours after administration of rVWF.
  • the dose and/or frequency of rVWF administration is such that the increase in FVIII half-life is maintained at least 5-125, 10-115, 15-105, 20-95, 25-85, 30-75, 35-65, 40-55 hours after administration ofrVWF.
  • rVWF is administered at a dose such that it increases the half-life of plasma FVIII by a value selected from variations 1046 to 1089 found in Table 7.
  • the rVWF of the invention shows an increased effect on the stability of FVIII as compared to the effect of pdVWF.
  • rVWF is administered at a dose and/or with a frequency such that it increases average FVIII half-life by about 1-15, 2-14, 3-13,4-12, 5-11, 6-10, 5-9, 6-8 hours.
  • rVWF is administered at a dose and/or frequency such that it increases FVIII half-life by about 10% to about 75% as compared to pdVWF.
  • rVWF increases FVIII half-life by about 10-80%, 15-65%, 20-60%, 25-55%, 30-50%, 35-45% as compared to pdVWF.
  • the average or percentage increase in FVIII half-life is maintained at least 10, 20, 30, 40, 50, 60, 70, 80, 90, 100 hours after administration of rVWF.
  • the increase in FVIII half-life is maintained at least 5-125, 10-115, 15-105, 20-95, 25-85, 30-75, 35-65, 40-55 hours after administration of rVWF.
  • the increase in FVIII stability, half-life and/or activity can be assessed using methods known in the art, including without limitation coagulation assays.
  • administration of rVWF increases the half-life of FVIII by an amount selected from variations 1300 to 1643 found in Table 9, as compared to administration of plasma-derived VWF.
  • the stabilization of FVIII activity by rVWF as compared to pdVWF can be measured by metrics in addition to FVIII half-life, including mean residence time (MRT) and area under curve (AUC).
  • MRT mean residence time
  • AUC area under curve
  • rVWF is administered at a dose and/or frequency such that it increases MRT by about 1-15 hours as compared to pdVWF.
  • rVWF increases MRT by about 1-25, 2-20, 3-15, 4-10, 5-9, 6-8 hours as compared to pdVWF.
  • rVWF increases FVIII MRT by about 10-80%, 15-65%, 20-60%, 25-55%, 30-50%, 35-45% as compared to pdVWF.
  • the average or percentage increase in FVIII half-life is maintained at least 10, 20, 30, 40, 50, 60, 70, 80, 90, 100 hours after administration of rVWF.
  • the increase in MRT is maintained at least 5-125, 10-115, 15-105, 20-95, 25-85, 30-75, 35-65, 40-55 hours after administration of rVWF.
  • administration of rVWF increases the MRT of FVIII by an amount selected from variations 1300 to 1643 found in Table 9, as compared to administration of plasma-derived VWF.
  • the doses of rVWF administered to patients are comparable to doses used in administration of pdVWF/pdFVIII.
  • compositions of rVWF with or without FVIII can be contained in pharmaceutical formulations, as described herein. Such formulations can be administered orally, topically, transdermally, parenterally, by inhalation spray, vaginally, rectally, or by intracranial injection.
  • parenteral as used herein includes subcutaneous injections, intravenous, intramuscular, intracisternal injection, or infusion techniques. Administration by intravenous, intradermal, intramusclar, intramammary, intraperitoneal, intrathecal, retrobulbar, intrapulmonary injection and or surgical implantation at a particular site is contemplated as well.
  • compositions are essentially free of pyrogens, as well as other impurities that could be harmful to the recipient.
  • formulations of the invention are administered by an initial bolus followed by a continuous infusion to maintain therapeutic circulating levels of drug product.
  • the inventive compound is administered as a one-time dose.
  • the route of administration can be, but is not limited to, by intravenous, intraperitoneal, subcutaneous, or intramuscular administration.
  • the frequency of dosing depends on the pharmacokinetic parameters of the agents and the route of administration.
  • the optimal pharmaceutical formulation is determined by one skilled in the art depending upon the route of administration and desired dosage. See for example, Remington's Pharmaceutical Sciences, 18th Ed., 1990, Mack Publishing Co., Easton, Pa.
  • Such formulations influence the physical state, stability, rate of in vivo release, and rate of in vivo clearance of the administered agents.
  • a suitable dose is calculated according to body weight, body surface area or organ size.
  • Appropriate dosages may be ascertained through use of established assays for determining blood level dosages in conjunction with appropriate dose-response data.
  • the final dosage regimen is determined by the attending physician, considering various factors which modify the action of drugs, e.g. the drug's specific activity, the severity of the damage and the responsiveness of the patient, the age, condition, body weight, sex and diet of the patient, the severity of any infection, time of administration and other clinical factors.
  • a typical dose of a recombinant VWF of the present invention is approximately 50 U/kg, equal to 500 ā‡ g/kg.
  • rVWF is administered to a subject alone. In some embodiments, rVWF is administered to a subject in combination with one or more coagulation factors. In further embodiments, the coagulation factor administered with rVWF is FVIII. In still further embodiments rVWF is administered prior to, subsequent to, or simultaneously with a coagulation factor such as FVIII. In certain embodiments, rVWF and FVIII are administered together in a single composition. As will be appreciated, the FVIII that is co-administered with rVWF can be either recombinant FVIII or plasma derived.
  • rVWF (with or without FVIII) is administered to a subject no more than once daily. In further embodiments, rVWF (with or without FVIII) is administered to a subject: no more than once every other day, no more than once every third day, no more than once every fourth day, no more than once every fifth day, no more than once a week, no more than once every two weeks, no more than once a month. In still further embodiments, rVWF (with or without FVIII) is administered to a subject no more than twice a day.
  • rVWF and FVIII are administered together to a subject in an initial dose, and then subsequent re-dosing is conducted with rVWF alone. In other embodiments, re-dosing is conducted with both rVWF and FVIII.
  • rVWF (with or without rFVIII) is administered at a dose such that plasma FVIII activity is stabilized for about 10 to about 90 hours. In further embodiments, plasma FVIII activity is stabilized for at least 12, 24, 36, 48 or 72 hours. As will be appreciated, the stabilized plasma FVIII activity may be that of endogenous FVIII, co-administered FVIII (plasma-derived or recombinant) or a combination of both endogenous and co-administered FVIII.
  • rVWF and FVIII are administered together at a dose such that extension of in vivo half-life of plasma FVIII activity is stabilized for at least 12, 24, 36, 48 or 72 hours. In further embodiments, the plasma FVIII activity is stabilized for about 10 to about 90 hours. In still further embodiments, the increase in half-life of plasma FVIII is maintained for at least 24, 36, 48, 72, 90, 120, or 168 hours in a patient.
  • the co-administered FVIII can be rFVIII or pdFVIII. In some embodiments, plasma FVIII activity is stabilized for a time selected from variations 1090 to 1299 found in Table 8, after co-administration of rVWF and FVIII.
  • the present invention provides methods for treating von Willebrand Disease (VWD).
  • VWD von Willebrand Disease
  • hemophilia refers to a group of disease states broadly characterized by reduced blood clotting or coagulation. Hemophilia may refer to Type A, Type B, or Type C hemophilia, or to the composite of all three diseases types.
  • Type A hemophilia (hemophilia A) is caused by a reduction or loss of factor VIII (FVIII) activity and is the most prominent of the hemophilia subtypes.
  • Type B hemophilia results from the loss or reduction of factor IX (FIX) clotting function.
  • Type C hemophilia is a consequence of the loss or reduction in factor XI (FXI) clotting activity.
  • Hemophilia A and B are X-linked diseases, while hemophilia C is autosomal.
  • Common treatments for hemophilia include both prophylactic and on-demand administration of clotting factors, such as FVIII, FIX, including BebulinĀ®-VH, and FXI, as well as FEIBA-VH, desmopressin, and plasma infusions.
  • von Willebrand Disease refers to the group of diseases caused by a deficiency of von Willebrand factor. Von Willebrand factor helps blood platelets clump together and stick to the blood vessel wall, which is necessary for normal blood clotting. There are several types of Von Willebrand disease.
  • Type Characteristics Quantitative forms of VWD Type 1 ā€¢ Partial quantitative deficiencies of VWF ā€¢ VWF plasma levels that are 5% to 30% of normal ā€¢ approximately 60% to 80% of patients Type 3 ā€¢ Virtually complete deficiency of VWF ā€¢ Approximately 1 % to 5% of patients Qualitative forms of VWD Type 2 Approximately 10% to 30% of patients Type 2A ā€¢ Decreased VWF-dependent platelet adhesion ā€¢ Selective deficiency of HMW-VMF multimers ā€¢ Platelet binding functions of VWF are impaired Type 2B ā€¢ Gain of function mutation with increased VWF binding to platelets ā€¢ Loss of HMW- VWF multimers from plasma, but not from platelets ā€¢ Loss of both VWF and platelets through a clearance mechanism Type 2M ā€¢ Decreased VWF-dependent platelet adhesion without selective deficiency of HMW-VWF multimers Type 2N ā€¢ Markedly decreased binding affinity for factor VIII Adopted from Sadler, J Thromb Haemost 2006; 4, 2103
  • Methods for treating coagulation disease include administering rVWF or a combination of rVWF rFVIII to subjects in need thereof in accordance with any of the methods of administration described herein and known in the art.
  • rVWF (with or without rFVIII) is administered to a subject such that the level of Factor VIII procoagulant activity (FVIII:C) in the plasma of the subject 24, 36, 48 or more hours post-administration is at least 90% of the level of FVIII:C activity present in the plasma 1 hour post-administration.
  • the level of the FVIII:C in the plasma of the subject 24, 36, 48 or more hours post-administration is at least between 50% and 1 00% of the level of FVIII:C activity present in the plasma 1 hour post-administration.
  • the level of the FVIII:C in the plasma of the subject 24, 36, 48 or more hours post-administration is at least 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98%, 99%, 100% of the level of FVIII:C activity present in the plasma 1 hour post-administration.
  • the present disclosure provides method for treating Von Willebrand Disease (VWD) in a subject in need thereof, which includes administering a composition of recombinant Von Willebrand Factor (rVWF) such that Factor VIII (FVIII) stability is increased, as compared to FVIII half-life in a subject administered a composition of plasma derived Von Willebrand Factor (pdVWF).
  • rVWF recombinant Von Willebrand Factor
  • pdVWF plasma derived Von Willebrand Factor
  • the composition of rVWF administered to the subject is a composition of high molecular weight rVWF multimers.
  • the composition of rVWF administered to the subject has a higher specific activity than a composition of pdVWF.
  • the composition of rVWF administered to the subject is a composition of high molecular weight rVWF multimers with a higher specific activity than a composition of pdVWF.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII.
  • the method is for treating any type of VWD. In a specific embodiment, the method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF such that FVIII stability is extended by at least 10%, 20%, 30%, 2 hr, 4 hr, 6 hr, or by an amount selected from variations 1300 to 1643 found in Table 9, as compared to FVIII stability in a subject administered a composition of pdVWF.
  • the composition of rVWF administered to the subject is a composition of high molecular weight rVWF multimers.
  • the composition of rVWF administered to the subject has a higher specific activity than a composition of pdVWF.
  • the composition of rVWF administered to the subject is a composition of high molecular weight rVWF multimers with a higher specific activity than a composition of pdVWF.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF such that FVIII stability is extended by at least 10% as compared to FVIII stability in a subject administered a composition of pdVWF, wherein the composition of rVWF administered to the subject is a composition of high molecular weight rVWF multimers having a minimal percentage of rVWF molecules present in a particular higher-order rVWF multimer or larger multimer according to any one of variations 134 to 457 found in Table 3 to Table 5.
  • the composition of rVWF administered to the subject has a higher specific activity than a composition of pdVWF.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF such that FVIII stability is extended by at least 20% as compared to FVIII stability in a subject administered a composition of pdVWF, wherein the composition of rVWF administered to the subject is a composition of high molecular weight rVWF multimers having a minimal percentage of rVWF melecules present in a particular higher-order rVWF multimer or larger multimer according to any one of variations 134 to 457 found in Table 3 to Table 5.
  • the composition of rVWF administered to the subject has a higher specific activity than a composition of pdVWF.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF such that FVIII stability is extended by at least 30% as compared to FVIII stability in a subject administered a composition of pdVWF, wherein the composition of rVWF administered to the subject is a composition of high molecular weight rVWF multimers having a minimal percentage of rVWF molecules present in a particular higher-order rVWF multimer or larger multimer according to any one of variations 134 to 457 found in Table 3 to Table 5.
  • the composition of rVWF administered to the subject has a higher specific activity than a composition of pdVWF.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF, wherein the combination of rVWF specific activity in the composition and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF, is selected from variations 2339 to 4868 in Table 13 to Table 19.
  • the composition of rVWF administered to the subject is a composition of high molecular weight rVWF multimers.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF, wherein the composition of rVWF administered to the subject is a composition of high molecular weight rVWF multimers in which at least 40% of rVWF molecules in the composition are present in a multimer of at least 10 subunits, and wherein the combination of rVWF specific activity in the composition and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF, is selected from variations 2339 to 4868 in Table 13 to Table 19.
  • the composition of rVWF administered to the subject is a composition of high molecular weight rVWF multimers.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII.
  • the method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF, wherein the composition of rVWF administered to the subject is a composition of high molecular weight rVWF multimers in which at least 50% of rVWF molecules in the composition are present in a multimer of at least 10 subunits, and wherein the combination of rVWF specific activity in the composition and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF, is selected from variations 2339 to 4868 in Table 13 to Table 19.
  • the composition of rVWF administered to the subject is a composition of high molecular weight rVWF multimers.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII.
  • the method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF, wherein the composition of rVWF administered to the subject is a composition of high molecular weight rVWF multimers in which at least 70% of rVWF molecules in the composition are present in a multimer of at least 10 subunits, and wherein the combination of rVWF specific activity in the composition and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF, is selected from variations 2339 to 4868 in Table 13 to Table 19.
  • the composition of rVWF administered to the subject is a composition of high molecular weight rVWF multimers.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII.
  • the method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF, wherein the composition of rVWF administered to the subject is a composition of high molecular weight rVWF multimers having a minimal percentage of rVWF molecules present in a particular higher-order rVWF multimer or larger multimer according to any one of variations 134 to 457 found in Table 3 to Table 5, and wherein the combination of rVWF specific activity in the composition and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF, is selected from variations 2339 to 4868 in Table 13 to Table 19.
  • the composition of rVWF administered to the subject is a composition of high molecular weight rVWF multimers.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII.
  • the method is for treating any type of VWD. The method is for treating Type 3 VWD.
  • the method comprises administering a dosage of a rVWF composition containing from 10 IU/kg to 40 IU/kg rVWF:RCo activity, wherein the combination of rVWF specific activity in the composition and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF, is selected from variations 2339 to 4868 in Table 13 to Table 19.
  • the composition contains from 20 IU/kg to 30 IU/kg rVWF:RCo activity.
  • the composition of rVWF administered to the subject is a composition of high molecular weight rVWF multimers.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII.
  • the method is for treating Type 3 VWD.
  • the method comprises administering a dosage of a rVWF composition containing from 25 IU/kg to 75 IU/kg rVWF:RCo activity, wherein the combination of rNWF specific activity in the composition and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF, is selected from variations 2339 to 4868 in Table 13 to Table 19.
  • the composition contains from 40 IU/kg to 60 IU/kg rVWF:RCo activity.
  • the composition of rVWF administered to the subject is a composition of high molecular weight rVWF multimers.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a dosage of a rVWF composition containing from 75 IU/kg to 125 IU/kg rVWF:RCo activity, wherein the combination of rVWF specific activity in the composition and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF, is selected from variations 2339 to 4868 in Table 13 to Table 19.
  • the composition contains from 75 IU/kg to 100 IU/kg rVWF:RCo activity.
  • the composition of rVWF administered to the subject is a composition of high molecular weight rVWF multimers.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF, wherein the subject is administered a dose of RVWF selected from variations 2141 to 2338 in Table 12, and wherein the combination of rVWF specific activity in the composition and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF, is selected from variations 2339 to 4868 in Table 13 to Table 19.
  • the composition of rVWF administered to the subject is a composition of high molecular weight rVWF multimers.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF, wherein the dose of rVWF and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF, is selected from variations 4869 to 8003 in Table 20 to Table 27.
  • the composition of rVWF administered to the subject is a composition of high molecular weight rVWF multimers.
  • the composition of rVWF administered to the subject has a higher specific activity than a composition of pdVWF.
  • the composition of rVWF administered to the subject is a composition of high molecular weight rVWF multimers with a higher specific activity than a composition of pdVWF.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF, wherein the composition of rVWF administered to the subject is a composition of high molecular weight rVWF multimers in which at least 40% of rVWF molecules in the composition are present in a multimer of at least 10 subunits, and wherein the dose of rVWF and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF, is selected from variations 4869 to 8003 in Table 20 to Table 27.
  • the composition of rVWF administered to the subject has a higher specific activity than a composition of pdVWF.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF, wherein the composition of rVWF administered to the subject is a composition of high molecular weight rVWF multimers in which at least 50% of rVWF molecules in the composition are present in a multimer of at least 10 subunits, and wherein the dose of rVWF and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF, is selected from variations 4869 to 8003 in Table 20 to Table 27.
  • the composition of rVWF administered to the subject has a higher specific activity than a composition of pdVWF.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF, wherein the composition of rVWF administered to the subject is a composition of high molecular weight rVWF multimers in which at least 70% of rVWF molecules in the composition are present in a multimer of at least 10 subunits, and wherein the dose of rVWF and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF, is selected from variations 4869 to 8003 in Table 20 to Table 27.
  • the composition of rVWF administered to the subject has a higher specific activity than a composition of pdVWF.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF, wherein the composition of rVWF administered to the subject is a composition of high molecular weight rVWF multimers having a minimal percentage of rVWF molecules present in a particular higher-order rVWF multimer or larger multimer according to any one of variations 134 to 457 found in Table 3 to Table 5, and wherein the dose of rVWF and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF, is selected from variations 4869 to 8003 in Table 20 to Table 27.
  • the composition of rVWF administered to the subject has a higher specific activity than a composition of pdVWF.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII.
  • the method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF, wherein the rVWF in the composition has a specific activity of from 40 mU/ ā‡ g to 60 mU/ ā‡ g, and wherein the dose of rVWF and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF, is selected from variations 4869 to 8003 in Table 20 to Table 27.
  • the composition of rVWF administered to the subject is a composition of high molecular weight rVWF multimers.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF, wherein the rVWF in the composition has a specific activity of at least 60 mU/ ā‡ g, and wherein the dose of rVWF and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF, is selected from variations 4869 to 8003 in Table 20 to Table 27.
  • the composition of rVWF administered to the subject is a composition of high molecular weight rVWF multimers.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF, wherein the rVWF in the composition has a specific activity of at least 80 mU/ ā‡ g, and wherein the dose of rVWF and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF, is selected from variations 4869 to 8003 in Table 20 to Table 27.
  • the composition of rVWF administered to the subject is a composition of high molecular weight rVWF multimers.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF, wherein the rVWF in the composition has a specific activity selected from variations 1 to 133 found in Table 1, and wherein the dose of rVWF and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF, is selected from variations 4869 to 8003 in Table 20 to Table 27.
  • the composition of rVWF administered to the subject is a composition of high molecular weight rVWF multimers.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF, wherein the dose of rVWF and specific activity of rVWF in the composition is selected from variations 8004 to 10625 in Table 28 to Table 34.
  • the composition of rVWF administered to the subject is a composition of high molecular weight rVWF multimers.
  • the composition of rVWF administered to the subject has a higher specific activity than a composition of pdVWF.
  • the composition of rVWF administered to the subject is a composition of high molecular weight rVWF multimers with a higher specific activity than a composition of pdVWF.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF, wherein the composition of rVWF administered to the subject is a composition of high molecular weight rVWF multimers in which at least 30% of rVWF molecules in the composition are present in a multimer of at least 10 subunits, and wherein the dose of rVWF and specific activity of rVWF in the composition is selected from variations 8004 to 10625 in Table 28 to Table 34.
  • the composition of rVWF administered to the subject has a higher specific activity than a composition of pdVWF.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF, wherein the composition of rVWF administered to the subject is a composition of high molecular weight rVWF multimers in which at least 50% of rVWF molecules in the composition are present in a multimer of at least 10 subunits, and wherein the dose of rVWF and specific activity of rVWF in the composition is selected from variations 8004 to 10625 in Table 28 to Table 34.
  • the composition of rVWF administered to the subject has a higher specific activity than a composition of pdVWF.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF, wherein the composition of rVWF administered to the subject is a composition of high molecular weight rVWF multimers in which at least 70% of rVWF molecules in the composition are present in a multimer of at least 10 subunits, and wherein the dose of rVWF and specific activity of rVWF in the composition is selected from variations 8004 to 10625 in Table 28 to Table 34.
  • the composition of rVWF administered to the subject has a higher specific activity than a composition of pdVWF.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF, wherein the composition of rVWF administered to the subject is a composition of high molecular weight rVWF multimers having a minimal percentage of rVWF molecules present in a particular higher-order rVWF multimer or larger multimer according to any one of variations 134 to 457 found in Table 3 to Table 5, and wherein the dose of rVWF and specific activity of rVWF in the composition is selected from variations 8004 to 10625 in Table 28 to Table 34.
  • the composition of rVWF administered to the subject has a higher specific activity than a composition of pdVWF.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF, wherein FVIII in the subject is stabilized for at least 18 hours post-administration, and wherein the dose of rVWF and specific activity of rVWF in the composition is selected from variations 8004 to 10625 in Table 28 to Table 34.
  • the composition of rVWF administered to the subject has a higher specific activity than a composition of pdVWF.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF, wherein FVIII in the subject is stabilized for at least 24 hours post-administration, and wherein the dose of rVWF and specific activity of rVWF in the composition is selected from variations 8004 to 10625 in Table 28 to Table 34.
  • the composition of rVWF administered to the subject has a higher specific activity than a composition of pdVWF.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF, wherein FVIII in the subject is stabilized for at least 30 hours post-administration, and wherein the dose of rVWF and specific activity of rVWF in the composition is selected from variations 8004 to 10625 in Table 28 to Table 34.
  • the composition of rVWF administered to the subject has a higher specific activity than a composition of pdVWF.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the present disclosure provides method for treating Von Willebrand Disease (VWD) in a subject in need thereof, which includes administering a composition of recombinant Von Willebrand Factor (rVWF) and recombinant FVIII (rFVIII) such that Factor VIII (FVIII) stability is increased, as compared to FVIII half-life in a subject administered a composition of plasma derived Von Willebrand Factor (pdVWF).
  • the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers.
  • the composition of rVWF/rFVHI administered to the subject has a higher VWF specific activity than a composition of pdVWF.
  • the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers with a higher VWF specific activity than a composition of pdVWF.
  • FVIII stability is characterized by the half life of FV III.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII such that FVIII stability is extended by at least 10%, 20%, 30%, 2 hr, 4 hr, 6 hr, or by an amount selected from variations 1300 to 1643 found in Table 9, as compared to FVIII stability in a subject administered a composition of pdVWF/FVIII.
  • the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers.
  • the composition of rVWF/rFVIII administered to the subject has a higher VWF specific activity than a composition of pdVWF/FVIII.
  • the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers with a higher specific activity than a composition of pdVWF.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII such that FVIII stability is extended by at least 10% as compared to FVIII stability in a subject administered a composition of pdVWF/FVIII, wherein the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers having a minimal percentage of rVWF molecules present in a particular higher-order rVWF multimer or larger multimer according to any one of variations 134 to 457 found in Table 3 to Table 5.
  • the composition of rVWF/rFVIII administered to the subject has a higher VWF specific activity than a composition of pdVWF/FVIII.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII such that FVIII stability is extended by at least 20% as compared to FVIII stability in a subject administered a composition of pdVWF/FVIII, wherein the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers having a minimal percentage of rVWF molecules present in a particular higher-order rVWF multimer or larger multimer according to any one of variations 134 to 457 found in Table 3 to Table 5.
  • the composition of rVWF/rFVIII administered to the subject has a higher VWF specific activity than a composition of pdVWF/FVIII.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII such that FVIII stability is extended by at least 30% as compared to FVIII stability in a subject administered a composition of pdVWF/FVIII, wherein the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers having a minimal percentage of rVWF molecules present in a particular higher-order rVWF multimer or larger multimer according to any one of variations 134 to 457 found in Table 3 to Table 5.
  • the composition of rVWF/rFVIII administered to the subject has a higher specific activity than a composition of pdVWF/FVMI.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the combination of rVWF specific activity in the composition and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF/FVIII, is selected from variations 2339 to 4868 in Table 13 to Table 19.
  • the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. : The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers in which at least 30% of rVWF molecules in the composition are present in a multimer of at least 10 subunits, and wherein the combination of rVWF specific activity in the composition and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF/FVIII, is selected from variations 2339 to 4868 in Table 13 to Table 19.
  • the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers in which at least 50% of rVWF molecules in the composition are present in a multimer of at least 10 subunits, and wherein the combination of rVWF specific activity in the composition and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF/FVIII, is selected from variations 2339 to 4868 in Table 13 to Table 19.
  • the composition of rWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers in which at least 70% of rVWF molecules in the composition are present in a multimer of at least 10 subunits, and wherein the combination of rVWF specific activity in the composition and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF/FVIII, is selected from variations 2339 to 4868 in Table 13 to Table 19.
  • the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers having a minimal percentage of rVWF molecules present in a particular higher-order rVWF multimer or larger multimer according to any one of variations 134 to 457 found in Table 3 to Table 5, and wherein the combination of rVWF specific activity in the composition and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF/FVIII, is selected from variations 2339 to 4868 in Table 13 to Table 19.
  • the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a dosage of a rVWF/rFVIII composition containing from 10 IU/kg to 40 IU/kg rVWF:RCo activity, wherein the combination of rVWF specific activity in the composition and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF/FVIII, is selected from variations 2339 to 4868 in Table 13 to Table 19.
  • the composition contains from 20 IU/kg to 30 IU/kg rVWF:RCo activity.
  • the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII.
  • the method is for treating Type 3 VWD.
  • the method comprises administering a dosage of a rVWF/rFVIII composition containing from 25 IU/kg to 75 IU/kg rVWF:RCo activity, wherein the combination of rVWF specific activity in the composition and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF/FVIII, is selected from variations 2339 to 4868 in Table 13 to Table 19.
  • the composition contains from 40 IU/kg to 60 IU/kg rVWF:RCo activity.
  • the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII.
  • the method is for treating Type 3 VWD.
  • the method comprises administering a dosage of a rVWF/rFVIII composition containing from 75 IU/kg to 125 IU/kg rVWF:RCo activity, wherein the combination of rVWF specific activity in the composition and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF/FVIII, is selected from variations 2339 to 4868 in Table 13 to Table 19.
  • the composition contains from 75 IU/kg to 100 IU/kg rVWF:RCo activity.
  • the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII.
  • the method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the subject is administered a dose of rVWF selected from variations 2141 to 2338 in Table 12, and wherein the combination of rVWF specific activity in the composition and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF/FVIII, is selected from variations 2339 to 4868 in Table 13 to Table 19.
  • the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the dose of rVWF and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF/FVIII, is selected from variations 4869 to 8003 in Table 20 to Table 27.
  • the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers.
  • the composition of rVWF/rFVIII administered to the subject has a higher specific activity than a composition of pdVWF.
  • the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers with a higher specific activity than a composition of pdVWF/FVIII.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers in which at least 30% of rVWF molecules in the composition arc present in a multimer of at least 10 subunits, and wherein the dose of rVWF and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF/FVIII, is selected from variations 4869 to 8003 in Table 20 to Table 27.
  • the composition of rVWF/rFVIII administered to the subject has a higher specific activity than a composition of pdVWF/FVIII,
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers in which at least 50% of rVWF molecules in the composition are present in a multimer of at least 10 subunits, and wherein the dose of rVWF and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF/FVIII, is selected from variations 4869 to 8003 in Table 20 to Table 27.
  • the composition of rVWF/rFVIII administered to the subject has a higher specific activity than a composition of pdVWF/FVIII.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers in which at least 70% of rVWF molecules in the composition are present in a multimer of at least 10 subunits, and wherein the dose of rVWF and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF/FVIII, is selected from variations 4869 to 8003 in Table 20 to Table 27.
  • the composition of rVWF/rFVIII administered to the subject has a higher specific activity than a composition of pdVWF/FVIII.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers having a minimal percentage of rVWF molecules present in a particular higher-order rVWF multimer or larger multimer according to any one of variations 134 to 457 found in Table 3 to Table 5, and wherein the dose of rVWF and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF/FVIII, is selected from variations 4869 to 8003 in Table 20 to Table 27.
  • the composition of rVWF/rFVIII administered to the subject has a higher specific activity than a composition of pdVWF/FVIII.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the rVWF in the composition has a specific activity of from 40 mU/ ā‡ g to 60 mU/ ā‡ g, and wherein the dose of rVWF and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF/FVIII, is selected from variations 4869 to 8003 in Table 20 to Table 27.
  • the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the rVWF in the composition has a specific activity of at least 60 mU/ ā‡ g, and wherein the dose of rVWF and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF/FVIII, is selected from variations 4869 to 8003 in Table 20 to Table 27.
  • the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the rVWF in the composition has a specific activity of at least 80 mU/ ā‡ g, and wherein the dose of rVWF and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF/FVIII, is selected from variations 4869 to 8003 in Table 20 to Table 27.
  • the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the rVWF in the composition has a specific activity selected from variations 1 to 133 found in Table 1, and wherein the dose of rVWF and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF/FVIII, is selected from variations 4869 to 8003 in Table 20 to Table 27.
  • the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII.
  • the method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the dose of rVWF and specific activity of rVWF in the composition is selected from variations 8004 to 10625 in Table 28 to Table 34.
  • the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers.
  • the composition of rVWF/rFVIII administered to the subject has a higher specific activity than a composition of pdVWF/FVIII.
  • the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers with a higher VWF specific activity than a composition of pdVWF/FVIII.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers in which at least 40% of rVWF molecules in the composition are present in a multimer of at least 10 subunits, and wherein the dose of rVWF and specific activity of rVWF in the composition is selected from variations 8004 to 10625 in Table 28 to Table 34.
  • the composition of rVWF/rFVIII administered to the subject has a higher VWF specific activity than a composition of pdVWF/FVIII.
  • FVIII stability is characterized by the half life of FVIII. In another embodiment, FVIII stability is characterized by mean residence time (MRT) of FVIII. In a further embodiment, the method is for treating any type of VWD. In a specific embodiment, the method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers in which at least 50% of rVWF molecules in the composition are present in a multimer of at least 10 subunits, and wherein the dose of rVWF and specific activity of rVWF in the composition is selected from variations 8004 to 10625 in Table 28 to Table 34.
  • the composition of rVWF/rFVIII administered to the subject has a higher VWF specific activity than a composition of pdVWF/FVIII.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers in which at least 70% of rVWF molecules in the composition are present in a multimer of at least 10 subunits, and wherein the dose of rVWF and specific activity of rVWF in the composition is selected from variations 8004 to 10625 in Table 28 to Table 34.
  • the composition of rVWF/rFVIII administered to the subject has a higher VWF specific activity than a composition of pdVWF/FVIII.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers having a minimal percentage of rVWF molecules present in a particular higher-order rVWF multimer or larger multimer according to any one of variations 134 to 457 found in Table 3 to Table 5, and wherein the dose of rVWF and specific activity of rVWF in the composition is selected from variations 8004 to 10625 in Table 28 to Table 34.
  • the composition of rVWF/rFVIII administered to the subject has a higher VWF specific activity than a composition of pdVWF/FVIII.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein FVIII in the subject is stabilized for at least 18 hours post-administration, and wherein the dose of rVWF and specific activity of rVWF in the composition is selected from variations 8004 to 10625 in Table 28 to Table 34.
  • the composition of rVWF/rFVIII administered to the subject has a higher VWF specific activity than a composition of pdVWF/FVIII.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein FVIII in the subject is stabilized for at least 24 hours post-administration, and wherein the dose of rVWF and specific activity of rVWF in the composition is selected from variations 8004 to 10625 in Table 28 to Table 34.
  • the composition of rVWF/rFVIII administered to the subject has a higher VWF specific activity than a composition of pdVWF/FVIII.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein FVIII in the subject is stabilized for at least 30 hours post-administration, and wherein the dose of rVWF and specific activity of rVWF in the composition is selected from variations 8004 to 10625 in Table 28 to Table 34.
  • the composition of rVWF/rFVIII administered to the subject has a higher VWF specific activity than a composition of pdVWF/FVIII.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the ratio of rFVIII procoagulant activity (IU rFVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) in the composition is from 4:1-3:2, and wherein the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers having a minimal percentage of rVWF molecules present in a particular higher-order rVWF multimer or larger multimer according to any one of variations 134 to 457 found in Table 3 to Table 5.
  • the ratio of rFVIII procoagulant activity (IU rFVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) in the composition is from 3:1-3:2.
  • the composition of rVWF/rFVIII administered to the subject has a higher VWF specific activity than a composition of pdVWF/FVIII.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the ratio of rFVIII procoagulant activity (IU rFVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) in the composition is from 2:1-1:2, and wherein the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers having a minimal percentage of rVWF molecules present in a particular higher-order rVWF multimer or larger multimer according to any one of variations 134 to 457 found in Table 3 to Table 5.
  • the ratio of rFVIII procoagulant activity (IU rFVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) in the composition is from 3:2-2:3.
  • the composition of rVWF/rFVIII administered to the subject has a higher VWF specific activity than a composition of pdVWF/FVIII.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the ratio of rFVIII procoagulant activity (IU rFVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) in the composition is from 2:3-1:6, and wherein the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers having a minimal percentage of rVWF molecules present in a particular higher-order rVWF multimer or larger multimer according to any one of variations 134 to 457 found in Table 3 to Table 5.
  • the ratio of rFVIII procoagulant activity (IU rFVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) in the composition is from 2:3-1:5.
  • the composition of rVWF/rFVIII administered to the subject has a higher specific activity than a composition of pdVWF/FVIII.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the ratio of rFVIII procoagulant activity (IU rFVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) in the composition is selected from variations 1988 to 2140 found in Table 11, and wherein the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers having a minimal percentage of rVWF molecules present in a particular higher-order rVWF multimer or larger multimer according to any one of variations 134 to 457 found in Table 3 to Table 5.
  • the composition of rVWF/rFVIII administered to the subject has a higher VWF specific activity than a composition of pdVWF/FVIII.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the ratio of rFVIII procoagulant activity (IU rFVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) in the composition is selected from variations 1988 to 2140 found in Table 11.
  • the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII.
  • the method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the ratio of rFVIII procoagulant activity (IU rFVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) in the composition is from 4:1-3:2, and wherein the combination of rVWF specific activity in the composition and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF/FVIII, is selected from variations 2339 to 4868 in Table 13 to Table 19.
  • the ratio of rFVIII procoagulant activity (IU rFVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) in the composition is from 3:1-3:2.
  • the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the ratio of rFVIII procoagulant activity (IU rFVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) in the composition is from 2:1-1:2, and wherein the combination of rVWF specific activity in the composition and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF/FVIII, is selected from variations 2339 to 4868 in Table 13 to Table 19.
  • the ratio of rFVIII procoagulant activity (IU rFVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) in the composition is from 3:2-2:3.
  • the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the ratio of rFVIII procoagulant activity (IU rFVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) in the composition is from 2:3-1:6, and wherein the combination of rVWF specific activity in the composition and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF/FVIII, is selected from variations 2339 to 4868 in Table 13 to Table 19.
  • the ratio of rFVIII procoagulant activity (IU rFVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) in the composition is from 2:3-1:5.
  • the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the ratio of rFVIII procoagulant activity (IU rFVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) in the composition is selected from variations 1988 to 2140 found in Table 11, and wherein the combination of rVWF specific activity in the composition and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF/FVIII, is selected from variations 2339 to 4868 in Table 13 to Table 19.
  • the composition of rVWF/rFVIII administered to the subject is a composition of high molecular weight rVWF multimers.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the ratio of rFVIII procoagulant activity (IU rFVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) in the composition is from 4:1-3:2, and wherein the dose of rVWF and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF/FVIII, is selected from variations 4869 to 8003 in Table 20 to Table 27.
  • the ratio of rFVIII procoagulant activity (IU rFVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) in the composition is from 3:1-3:2.
  • the composition of rVWF/rFVIII administered to the subject has a higher specific activity than a composition of pdVWF/FVIII.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the ratio of rFVIII procoagulant activity (IU rFVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) In the composition is from 2:1-1:2, and wherein the dose of rVWF and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF/FVIII, is selected from variations 4869 to 8003 in Table 20 to Table 27.
  • the ratio of rFVIII procoagulant activity (IU rFVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) in the composition is from 3:2-2:3.
  • the composition of rVWF/rFVIII administered to the subject has a higher specific activity than a composition of pdVWF/FVIII.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the ratio of rFVIII procoagulant activity (IU rFVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF.RCo) in the composition is from 2:3-1:6, and wherein the dose of rVWF and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF/FVIII, is selected from variations 4869 to 8003 in Table 20 to Table 27.
  • the ratio of rFVIII procoagulant activity (IU rFVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) in the composition is from 2:3-1:5.
  • the composition of rVWF/rFVIII administered to the subject has a higher specific activity than a composition of pdVWF/FVIII.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the ratio of rFVIII procoagulant activity (IU rFVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) in the composition is selected from variations 1988 to 2140 found in Table 11, and wherein the dose of rVWF and increase in FVIII stability, as compared to FVIII stability in a subject administered a composition of pdVWF/FVIII, is selected from variations 4869 to 8003 in Table 20 to Table 27.
  • the ratio of rFVIII procoagulant activity IU rFVIII:C
  • rVWF Ristocetin cofactor activity IU rVWF:RCo
  • the composition of rVWF/rFVIII administered to the subject has a higher specific activity than a composition of pdVWF/FVIII.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the ratio of rFVIII procoagulant activity (IU rFVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) in the composition is from 4:1-3:2, and wherein the dose of rVWF and specific activity of rVWF in the composition is selected from variations 8004 to 10625 in Table 28 to Table 34.
  • the ratio of rFVIII procoagulant activity (IU rFVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) in the composition is from 3:1-3:2.
  • the composition of rVWF/rFVIII administered to the subject has a higher VWF specific activity than a composition of pdVWF/FVIII.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the ratio of rFVIII procoagulant activity (IU rFVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) in the composition is from 2:1-1:2, and wherein the dose of rVWF and specific activity of rVWF in the composition is selected from variations 8004 to 10625 in Table 28 to Table 34 .
  • the ratio of rFVIII procoagulant activity (IU rFVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) in the composition is from 3:2-2:3.
  • the composition of rVWF/rFVIII administered to the subject has a higher VWF specific activity than a composition of pdVWF/FVIII.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the ratio of rFVIII procoagulant activity (IU rFVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) in the composition is from 2:3-1:6, and wherein the dose of rVWF and specific activity of rVWF in the composition is selected from variations 8004 to 10625 in Table 28 to Table 34.
  • the ratio of rFVIII procoagulant activity (IU rFVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) in the composition is from 2:3-1:5.
  • the composition of rVWF/rFVIII administered to the subject has a higher VWF specific activity than a composition of pdVWF/FVIII.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the method comprises administering a composition of rVWF/rFVIII, wherein the ratio of rFVIII procoagulant activity (IU rFVIII:C) to rVWF Ristocetin cofactor activity (IU rVWF:RCo) in the composition is selected from variations 1988 to 2140 found in Table 11, and wherein the dose of rVWF and specific activity of rVWF in the composition is selected from variations 8004 to 10625 in Table 28 to Table 34.
  • the composition of rVWF/rFVIII administered to the subject has a higher VWF specific activity than a composition of pdVWF/FVIII.
  • FVIII stability is characterized by the half life of FVIII.
  • FVIII stability is characterized by mean residence time (MRT) of FVIII. The method is for treating Type 3 VWD.
  • the practice of the present invention may employ, unless otherwise indicated, conventional techniques and descriptions of organic chemistry, polymer technology, molecular biology (including recombinant techniques), cell biology, biochemistry, and immunology, which are within the skill of the art.
  • Such conventional techniques include polymer array synthesis, hybridization, ligation, and detection of hybridization using a label. Specific illustrations of suitable techniques can be had by reference to the example herein below. However, other equivalent conventional procedures can, of course, also be used.
  • Such conventional techniques and descriptions can be found in standard laboratory manuals such as Genome Analysis: A Laboratory Manual Series (Vols.
  • rVWF Von Willebrand Factor
  • VWF:RCo PK/VWF multimer kinetics showed highly similar PK.
  • VWF:RCo (VWF activity) between rVWF and Humate P FIG. 2A ).
  • Humate P is human derived medium purity Factor VIII concentrates complexed to VWF.
  • a surrogate marker was used for efficacy and dosing recommendations.
  • the data in FIG. 2A show that rVWF shows similar activity to that of plasma derived VW. Progressive loss of high molecular weight rVWF was seen upon exposure to ADAMTS13 ( FIG. 2B ), showing that rVWF is present in high molecular weight multimers prior to the ADAMTS13 exposure.
  • Ultra-large molecular weight multimers are present with rVWF - these ultra-large molecular weight multimers rapidly disappear following infusion. ADAMTS13 mediated cleavage fragments were seen in all subjects.
  • the pharmacokinetic profile of VWF:RCo was similar to that of pdVWF.
  • There was sustained stabilization of endogenous FVIII with rVWF which was comparable to that observed with pdVWF.
  • the adverse drug reaction profile with rVWF was similar to that of pdVWF/pdFVIII, and all related adverse events (AEs) were mild.
  • rVWF can be used for the treatment and preventing of bleeding episodes at doses comparable to pdVWF/pdFVIII, while enhancing the levels of FVIII as compared to the effect from the use of pdVWF.
  • the high proportion of ultra-large multimers (decamers or higher) in the population of rVWF leads to the enhanced stabilization of FVIII seen with rVWF as compared to that by plasma derived VWF.
  • the pdVWF used In this study was synthesized in endothelial cells and megakaryocytes. Post-translational modification of propeptide removal occurred intracellularly during passage of the protein to the Golgi and post-Golgi compartments. Glycosylation/ABO blood group glycans were present.
  • the pdVWF consisted of VWF subunits that had been exposed to plasma ADAMTS13, There were no ultra-large VWF multimers in the pdVWF population and subunits were cleaved at TYR 1605 -MET 1606 .
  • the rVWF used In this study was expressed in CHO cells. Propeptide removal was mediated in vitro through exposure of the pro-VWF to recombinant Furin. Fully glycosylated/ABO blood group glycans were absent. The rVWF was not exposed to ADAMTS13. The subunits of the rVWF were intact and ultra-large VWF multimers were present. Subunit cleavage did occur upon ADAMTS13 exposure. The rVWF showed higher specific activity than pdVWF.
  • FIG. 7 Further pharmacokinetic analysis of Cohort 4A (Type 3 VWD) FVIII:C is shown in FIG. 7 .
  • the data in FIG. 7 suggests that rVWF was more effective at stabilizing the in vivo activity of FVIII than pdVWF, resulting in increased FVIII procoagulant activity after treatment with rVWF/rVWF as compared to treatment with pdVWF/pdFVIII.
  • rVWF can be used for the treatment and preventing of bleeding episodes at doses comparable to pdVWF/pdFVIII.
  • FIG. 9 shows the rVWF PK parameters for three patients in the study.
  • FIG. 10 shows PK data for Patient 1.
  • VWF:RCo and VWF:CBA. Activities were measurable up to 12 hours (both were below the limit of quantification at 24 hours).
  • VWF:Ag was still measurable at 96 hours. Endogenous FVIII activity increased to a maximum of 0.13 IU/mL.
  • FIG. 11 shows PK data in Patient 2.
  • VWF:RCo As with Patient 1, there was a good correlation between VWF:RCo and VWF:CBA. Both activities were measurable (albeit at the limit of quantification) up to 12 hours. VWF:Ag was still measurable at 72 hours (the 96 hour sample was not tested). Endogenous FVIII activity increased to a maximum of 0.18 IU/mL for this patient.
  • FIG. 12 shows PK data in Patient 3.
  • VWF:RCo activity was measurable up to 24 hours (albeit at the limit of quantification), while VWF:CBA was below LoQ at 24 hours.
  • VWF:Ag was still measurable up to 48 hours.
  • Endogenous FVIII activity increased to a maximum of 0.13 IU/mL for this patient.
  • FIG. 13 shows data comparing the VWF parameters and FVIII activity for the three patients. There was a good correlation see in all three patients for all parameters tested (VWF:RCo, VWF:CBA, VWF:Ag, and FVII:Chr activity).
  • rVWF had ā‡ 100% recovery in all patients.
  • the three patients showed slightly different rVWF PK.
  • VWF antigen there was a maximum 0.06 IU/ml 30 minutes after application of 21U VWF:RCo/kg followed by a steady decline.
  • FVIII activity the baseline FVIII activity increased to approximately 0.1 IU/ml 15 minutes after application of rVWF+rFVIII. Thereafter, activity further increased to 0.16 IU/m), reached a plateau at 3-6 hours that stayed up to 28 hours followed by a steady decline.
  • the delayed increase in FVIII indicates that the secondary rise was induced by rVWF.
  • FIG. 14 shows data for FVIII activity across all cohorts.
  • FIG. 15 shows data from Cohort 1 (2 IU/kg VWF:RCo/1.5 IU/kg FVIII). There was good correlation for all three patients in this cohort for all parameters tested.
  • FIG. 15 shows data from Cohort 2 (7.5 IU/kg VWF:RCo/5.8 IU/kg FVIII).
  • FIG. 16 shows the pharmacokinetics data for this cohort for FVIII:C.
  • FIG. 17 shows data for Cohort 3 (20 IU/kg VWF:RCo/15.4 IU/kg FVIII). These data show a comparison of plasma parameters for VWF and FVIII.
  • FIG. 18 shows the pharmacokinetics data for this cohort for FVIII:C.
  • FIG. 19 shows data for Cohort 4 (50 IU/kg VWF:RCo). FVIII dosing was 38.5 IU/kg rFVIII or 25 IU/kg pdFVIII. These data show that the parameters for rVWF are similar to those for pdVWF (Haemate), but that rVWF is more effective at stabilizing FVIII activity, resulting in an increase seen in FVIII activity as compared to that seen with pdVWF.
  • FIG. 20 shows a summary of pharmacokinetics data for this cohort for FVIII:C.
  • the population for the study is selected using the following criteria:
  • Subject participation is for 16 weeks with an overall study duration of 7 months.
  • the design of the study is a multicenter, uncontrolled, non randomized, open-label clinical study to assess safety, immediate tolerability and pharmacokinetics of rFVIII:rVWF in subjects with hereditary severe hemophilia A (FVIII:C ā‡ 1%).
  • the intra-individual pharmacokinetics are spaced at 5-14 days apart to ensure a "wash-out" period of at least 5 days and a timely completion of the study.
  • Safety analyses are performed separately once 6 subjects have been dosed with 10 IU/KG VWF:RCo rVWF and once 6 subjects have been dosed with 50 IU/KG VWF:RCo rVWF.
  • Subjects should not have received cryoprecipitate, fresh frozen plasma or other drugs interfering with VWF or FVIII PK for at least 5 days before either of the infusions.
  • FVIII activity is determined using both the chromogenic and one-stage aPTT-based assay methods performed at the local and central laboratory.
  • AE adverse event
  • hematology hematology
  • clinical chemistry vital signs, clinical chemistry, and hematology parameters are assessed pre-infusion and until 120 hours post-infusion.
  • the occurrence of AEs are continuously monitored for up to 2 hours post-infusion (rVWF treated subjects) and at various time points during the follow-up period.
  • DMC independent data monitoring committee
  • Pharmacokinetic primary endpoints for the study include: AUC 0 - ā‡ /Dose (area under the plasma concentration/time curve from time 0 to infinity); AUC 0-96h /Dose (area under the plasma concentration/time curve from time 0 to 96 hours): mean residence time (MRT); clearance (CL); T1/2 (elimination phase half-life); Volume of distribution at steady state (Vss) of VWF:RCo, VWF:Ag ,VWF:CB, and FVIII.
  • Analysis for pharmacokinetic primary endpoints include AUC 0-96h /Dose, AUC 0- ā‡ /Dose, MRT, CL, T 1/2 and Vss summarized per treatment group (50 IU/kg rFVIII (Advate) alone, 50 IU/kg rFVIII (Advate) premixed with rVWF at 10 IU/kg VWF:RCo, 50 IU/kg rFVIII (Advate) premixed with rVWF at 50 IU/kg VWF:RCo) by median and two-sided 95% CIs for the median, mean, standard deviation, coefficient of variation and geometric mean. Descriptive statistics (medians and ranges) are used to summarize VWF:RCo, VWF:Ag, VWF:CB and FVIII levels over time.
  • Safety primary endpoint includes: occurrence of treatment related AEs. Analysis of the safety primary endpoint includes the number and percentage of subjects who experience a treatment related AE. The number and rate of treatment related AEs are tabulated.
  • Pharmacokinetic secondary endpoints include: In vivo recovery (IVR) and incremental recovery OR) of FVIII, VWF:RCo, VWF:Ag and VWF:CB. Analysis of pharmacokinetic secondary endpoints includes determining IVR and IR of FVIII, VWF:RCo, VWF:Ag and VWF:CB by subject and summarizing by medians and ranges.
  • Safety secondary endpoints include: development of inhibitory and total binding anti-VWF antibodies, development of inhibitory antibodies to FVIII, development of antibodies to Chinese hamster ovary (CHO) proteins, mouse immunoglobulin G (IgG) and rFurin, occurrence of thrombotic events.
  • CHO Chinese hamster ovary
  • IgG mouse immunoglobulin G
  • rFurin occurrence of thrombotic events.
  • Safety secondary endpoints are analyzed by tabulating the number of subjects who experience an SAE and the number of SAEs .
  • the number of subjects who experience a treatment related AE and the number and rate of treatment related AEs are subcategorized for thrombotic events, inhibitory and total binding anti-VWF antibodies, inhibitory antibodies to FVIII, antibodies to Chinese hamster ovary (CHO) proteins, antibodies to mouse immunoglobulin G (IgG) and antibodies to rFurin.
  • a listing of all AEs are presented by subject identifier, age, sex, preferred term and reported term of the AE, duration, severity, seriousness, action taken, outcome, causality assessment, onset date, stop date and medication or non-drug therapy to treat the AE.
  • An overview table for AEs are provided, presenting the number of AEs, the number of subjects with AEs and the corresponding percent of subjects in total and by seriousness and relationship to treatment.
  • An additional summary table presents the total number of (mild, moderate, severe) AEs by system organ class and preferred term with relationship to treatment.

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Claims (5)

  1. Facteur Von Willebrand recombinant (rVWF) pour utilisation dans un procĆ©dĆ© pour traiter la maladie de Von Willebrand de type 3, dans lequel le rVWF est une composition multimĆØre VWF de poids molĆ©culaire Ć©levĆ© comprenant au moins 40 % de dĆ©camĆØres VWF ou de multimĆØres d'ordre supĆ©rieur.
  2. rVWF pour l'utilisation selon la revendication 1, dans lequel le rVWF est mƻri in vitro par traitement avec de la furine.
  3. rVWF pour l'utilisation selon la revendication 1 ou la revendication 2, dans lequel le rVWF n'est pas exposƩ Ơ de l'ADAMTS13 durant la production en culture cellulaire.
  4. rVWF pour l'utilisation selon l'une quelconque des revendications 1 Ơ 3, dans lequel le rVWF prƩsente une activitƩ spƩcifique de 20 Ơ 150 mU/mg plus ou moins 10 %, optionnellement de 30 Ơ 120 mU/mg plus ou moins 10 %.
  5. rVWF pour l'utilisation selon l'une quelconque des revendications 1 Ć  4, dans lequel la composition multimĆØre VWF de poids molĆ©culaire Ć©levĆ© comprend au moins 50 % de dĆ©camĆØres VWF ou de multimĆØres d'ordre supĆ©rieur, le plus prĆ©fĆ©rentiellement dans lequel la composition multimĆØre VWF de poids molĆ©culaire Ć©levĆ© comprend au moins 60 % de dĆ©camĆØres VWF ou de multimĆØres d'ordre supĆ©rieur.
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ES2657291T3 (es) * 2013-04-22 2018-03-02 Csl Ltd. Un complejo covalente de factor de von Willebrand y factor VIII asociado por un puente disulfuro
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FR3034669B1 (fr) 2015-04-07 2020-02-14 Laboratoire Francais Du Fractionnement Et Des Biotechnologies Nouvelle utilisation du facteur von willebrand
AU2017250570B2 (en) 2016-04-15 2024-07-25 Takeda Pharmaceutical Company Limited Method and apparatus for providing a pharmacokinetic drug dosing regiment
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PT3648788T (pt) 2017-07-07 2024-08-23 Takeda Pharmaceuticals Co Tratamento de hemorragia gastrointestinal em pacientes com doenƧa de von willebrand grave por administraĆ§Ć£o de fvw recombinante
BR112020000322A2 (pt) 2017-07-07 2020-07-14 Baxalta Incorporated uso de fator de von willebrand recombinante (rvwf)
MX2020008294A (es) 2018-02-06 2020-11-18 Ablynx Nv Metodos de tratamiento de episodio inicial de ttp con dominios variables simples de inmunoglobulina.
AU2019240135B2 (en) * 2018-03-21 2024-10-03 Takeda Pharmaceutical Company Limited Separation of VWF and VWF propeptide by chromatographic methods
SG11202108325YA (en) * 2019-02-01 2021-08-30 Takeda Pharmaceuticals Co Methods of prophylactic treatment using recombinant vwf (rvwf)
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JP2023514541A (ja) 2020-02-04 2023-04-06 ę­¦ē”°č–¬å“å·„ę„­ę Ŗ式会ē¤¾ ēµ„ę›ćˆļ½–ļ½—ļ½†ć®ęŠ•äøŽć«ć‚ˆć‚‹é‡ē—‡ć®ćƒ•ć‚©ćƒ³ćƒ“ć‚£ćƒ¬ćƒ–ćƒ©ćƒ³ćƒ‰ē—…ę‚£č€…ć«ćŠć‘ć‚‹éŽå¤šęœˆēµŒć®ę²»ē™‚
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